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CAS

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251569-86-5

Cyclobutanecarboxylic acid, 2-hydroxy-, ethyl ester, (1R,2S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

251569-86-5

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  • Cyclobutanecarboxylic acid, 2-hydroxy-, ethyl ester, (1R,2S)- (9CI)

    Cas No: 251569-86-5

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251569-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 251569-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,1,5,6 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 251569-86:
(8*2)+(7*5)+(6*1)+(5*5)+(4*6)+(3*9)+(2*8)+(1*6)=155
155 % 10 = 5
So 251569-86-5 is a valid CAS Registry Number.

251569-86-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl cyclobutanol 2-carboxylate

1.2 Other means of identification

Product number -
Other names (1R,2S)-2-Hydroxy-cyclobutanecarboxylic acid ethyl ester

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:251569-86-5 SDS

251569-86-5Downstream Products

251569-86-5Relevant articles and documents

Preparation and use of (S)-O-acetyllactyl chloride (Mosandl's reagent) as a chiral derivatizing agent

Buisson, Didier,Azerad, Robert

, p. 2997 - 3002 (1999)

(S)-O-Acetyllactyl chloride is used as a versatile chiral derivatizing agent for the chromatographic determination of the enantiomeric excesses of alcohols or amines. However, some precautions must be taken to avoid its racemization during preparation and use. In addition, the racemic counterpart of this reagent can be used to determine the best analytical separation conditions.

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