JPH0583534B2 - - Google Patents

Info

Publication number: JPH0583534B2
Authority: JP; Japan
Prior art keywords: cellulose; optical resolution; formula; chloropropionic; chloropropionic acid
Prior art date: 1985-03-15
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

JP5203985A

Other languages

English (en)

Japanese (ja)

Other versions

JPS61212539A (ja

Inventor

Akito Ichida

Ichiro Okamoto

Tooru Shibata

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Daicel Corp

Original Assignee

Daicel Chemical Industries Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1985-03-15

Filing date

1985-03-15

Publication date

1993-11-26

1985-03-15 Application filed by Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd

1985-03-15 Priority to JP5203985A priority Critical patent/JPS61212539A/ja

1986-09-20 Publication of JPS61212539A publication Critical patent/JPS61212539A/ja

1993-11-26 Publication of JPH0583534B2 publication Critical patent/JPH0583534B2/ja

Status Granted legal-status Critical Current

Links

GAWAYYRQGQZKCR-UHFFFAOYSA-N 2-chloropropionic acid Chemical class CC(Cl)C(O)=O GAWAYYRQGQZKCR-UHFFFAOYSA-N 0.000 claims description 9
229920002678 cellulose Polymers 0.000 claims description 6
239000001913 cellulose Substances 0.000 claims description 6
230000003287 optical effect Effects 0.000 claims description 6
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 3
238000000034 method Methods 0.000 claims description 3
239000000203 mixture Substances 0.000 claims description 3
229920002284 Cellulose triacetate Polymers 0.000 claims description 2
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
150000004676 glycans Chemical class 0.000 claims description 2
229920001282 polysaccharide Polymers 0.000 claims description 2
239000005017 polysaccharide Substances 0.000 claims description 2
239000004480 active ingredient Substances 0.000 claims 1
125000003118 aryl group Chemical group 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
239000003795 chemical substances by application Substances 0.000 claims 1
-1 2-isopropylphenyl α-chloropropionate Chemical compound 0.000 description 4
BWWXKHHVIAJJFM-UHFFFAOYSA-N 2-chloro-n-phenylpropanamide Chemical compound CC(Cl)C(=O)NC1=CC=CC=C1 BWWXKHHVIAJJFM-UHFFFAOYSA-N 0.000 description 2
238000004587 chromatography analysis Methods 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
238000004811 liquid chromatography Methods 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
230000005526 G1 to G0 transition Effects 0.000 description 1
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
235000004279 alanine Nutrition 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
238000005660 chlorination reaction Methods 0.000 description 1
VDCSGNNYCFPWFK-UHFFFAOYSA-N diphenylsilane Chemical compound C=1C=CC=CC=1[SiH2]C1=CC=CC=C1 VDCSGNNYCFPWFK-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
QKGYJVXSKCDGOK-UHFFFAOYSA-N hexane;propan-2-ol Chemical compound CC(C)O.CCCCCC QKGYJVXSKCDGOK-UHFFFAOYSA-N 0.000 description 1
230000006698 induction Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
230000001766 physiological effect Effects 0.000 description 1
238000003908 quality control method Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP5203985A 1985-03-15 1985-03-15 α−クロロプロピオン酸類の光学分割方法 Granted JPS61212539A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP5203985A JPS61212539A (ja)	1985-03-15	1985-03-15	α−クロロプロピオン酸類の光学分割方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP5203985A JPS61212539A (ja)	1985-03-15	1985-03-15	α−クロロプロピオン酸類の光学分割方法

Publications (2)

Publication Number	Publication Date
JPS61212539A JPS61212539A (ja)	1986-09-20
JPH0583534B2 true JPH0583534B2 (es)	1993-11-26

Family

ID=12903672

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP5203985A Granted JPS61212539A (ja)	1985-03-15	1985-03-15	α−クロロプロピオン酸類の光学分割方法

Country Status (1)

Country	Link
JP (1)	JPS61212539A (es)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
USRE43573E1 (en)	1997-02-24	2012-08-14	Genesis Microchip (Delaware) Inc.	Method and system for displaying an analog image by a digital display device

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0796503B2 (ja) *	1986-07-04	1995-10-18	ダイセル化学工業株式会社	α−置換酢酸エステル類の光学分割方法
CN113607840B (zh) *	2021-07-29	2023-06-30	山东京博农化科技股份有限公司	一种2-氯丙酸手性异构体的分离检测方法

1985
- 1985-03-15 JP JP5203985A patent/JPS61212539A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
USRE43573E1 (en)	1997-02-24	2012-08-14	Genesis Microchip (Delaware) Inc.	Method and system for displaying an analog image by a digital display device

Also Published As

Publication number	Publication date
JPS61212539A (ja)	1986-09-20

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