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88496-70-2

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88496-70-2 Usage

Chemical Properties

Colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 88496-70-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,9 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88496-70:
(7*8)+(6*8)+(5*4)+(4*9)+(3*6)+(2*7)+(1*0)=192
192 % 10 = 2
So 88496-70-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H9ClO3/c1-9-5(8)2-4(7)3-6/h4,7H,2-3H2,1H3/t4-/m1/s1

88496-70-2 Well-known Company Product Price

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  • TCI America

  • (M1483)  Methyl (R)-4-Chloro-3-hydroxybutyrate  >97.0%(GC)

  • 88496-70-2

  • 5g

  • 1,150.00CNY

  • Detail

88496-70-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (3R)-4-chloro-3-hydroxybutanoate

1.2 Other means of identification

Product number -
Other names (R)-Methyl 4-chloro-3-hydroxybutanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88496-70-2 SDS

88496-70-2Relevant articles and documents

Highly enantioselective bioreduction of prochiral ketones by stem and germinated plant of Brassica oleracea variety italica

Mohammadi, Mehdi,Yousefi, Maryam,Habibi, Zohreh

experimental part, p. 328 - 336 (2012/03/11)

An eco-friendly and environmentally benign asymmetric reduction of a broad range of prochiral ketones employing Brassica oleracea variety italica (stems and germinated plant) as a novel biocatalyst was developed. It was found that B. oleracea variety italica could be used effectively for enantioselective bioreduction in aqueous medium with moderate to excellent chemical yield and enantiomeric excess (ee). This process is more efficient and generates less waste than conventional chemical reagents or microorganisms. Both R- and S-configurations were obtained by these asymmetric reactions. The best ee were achieved for pyridine derivatives (92-99%). The ee in germinated plant reactions were significantly higher than those of stem reactions. The low cost and the easy availability of these biocatalysts suggest their possible use for large scale preparations of important chiral alcohols.

Tandem concurrent processes: One-pot single-catalyst biohydrogen transfer for the simultaneous preparation of enantiopure secondary alcohols

Bisogno, Fabricio R.,Lavandera, Ivan,Kroutil, Wolfgang,Gotor, Vicente

supporting information; scheme or table, p. 1730 - 1732 (2009/07/11)

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Sequential kinetic resolution catalyzed by halohydrin dehalogenase

Elenkov, Maja Majeric,Tang, Lixia,Hauer, Bernhard,Janssen, Dick B.

, p. 4227 - 4229 (2007/10/03)

(Chemical Equation Presented) A sequential kinetic resolution catalyzed by halohydrin dehalogenase was employed for the synthesis of two valuable enantiopure building blocks. Resolution of methyl 4-chloro-3-hydroxybutanoate methylester ((R,S)-2) with use of a Trp249Phe mutant of halohydrin dehalogenase yielded methyl 4-cyano-3-hydroxybutanoate methylester ((S)-4) with 96.8% ee (40% yield) and (S)-2 with 95.2% ee (41% yield). This reaction is carried out in aqueous solution under mild conditions and provides access to a useful statin side-chain building block.

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