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128110-37-2

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128110-37-2 Usage

Chemical Properties

Almost white crystalline powder

Uses

An antifungal antibiotic.

Check Digit Verification of cas no

The CAS Registry Mumber 128110-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,1,1 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 128110-37:
(8*1)+(7*2)+(6*8)+(5*1)+(4*1)+(3*0)+(2*3)+(1*7)=92
92 % 10 = 2
So 128110-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2.ClH/c7-5-3-1-2-4(5)6(8)9;/h4-5H,1-3,7H2,(H,8,9);1H/t4-,5+;/m1./s1

128110-37-2 Well-known Company Product Price

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  • Aldrich

  • (712205)  (1R,2S)-(−)-2-Amino-1-cyclopentanecarboxylic acid hydrochloride hemihydrate  98.0-102.0% (calc. on dry substance, AT)

  • 128110-37-2

  • 712205-200MG

  • 2,397.33CNY

  • Detail

128110-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2S)-(-)-2-Amino-1-cyclopentanecarboxylic acid hydrochloride

1.2 Other means of identification

Product number -
Other names (1R,2S)-CISPENTACIN HYDROCHLORIDE

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:128110-37-2 SDS

128110-37-2Relevant articles and documents

The first direct enzymatic hydrolysis of alicyclic β-amino esters: A route to enantiopure cis and trans β-amino acids

Forro, Eniko,Fueloep, Ferenc

, p. 6397 - 6401 (2008/02/13)

The first direct enzymatic method is reported for the synthesis of cis and trans βamino acid enantiomers through the lipase-catalyzed enantioselective hydrolysis of alicyclic β esters in organic media. High enantioselectivities (E usually > 001) were observed when the Candida antarctica lipase B catalyzed reactions were performed with H2O (0.5 equivalents) in iP iPr2O at 5°C. The resolved products, obtained in good yields (≥42%), could be easily separated.

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