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40125-55-1

40125-55-1

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40125-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40125-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,2 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40125-55:
(7*4)+(6*0)+(5*1)+(4*2)+(3*5)+(2*5)+(1*5)=71
71 % 10 = 1
So 40125-55-1 is a valid CAS Registry Number.

40125-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-5-methyloxolan-2-one

1.2 Other means of identification

Product number -
Other names DIHYDRO-5-CHLORO-5-METHYL-2(3H)-FURANONE

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:40125-55-1 SDS

40125-55-1Upstream product

40125-55-1Downstream Products

40125-55-1Relevant articles and documents

Glycoconjugates and use thereof as vaccine against Shigella flexneri serotype 3a and X

-

Page/Page column 162, (2014/09/03)

The present invention relates to compounds derived from sugars which reproduce the epitopes of Shigella flexneri serotypes 3a and X and to the use thereof for the preparation of vaccine compositions. More specifically, the subject matter of the present in

Radicals from aldehydes: A convergent access to dienes and δ-lactones

Bagal, Sharanjeet K.,Tournier, Lucie,Zard, Samir Z.

, p. 1485 - 1490 (2007/10/03)

A convenient method for the generation of O,S-acetal xanthates from aldehydes has been developed. The corresponding nucleophilic radicals undergo facile addition to unactivated olefins and the resulting adducts can be further elaborated to generate dienes

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