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137618-50-9

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137618-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137618-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,6,1 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 137618-50:
(8*1)+(7*3)+(6*7)+(5*6)+(4*1)+(3*8)+(2*5)+(1*0)=139
139 % 10 = 9
So 137618-50-9 is a valid CAS Registry Number.

137618-50-9SDS

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 Propanamide, 2,3-dihydroxy-N,N-dimethyl- (9CI)

1.2 Other means of identification

Product number -
Other names 2,3-dihydroxy-N,N-dimethylpropionamide

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:137618-50-9 SDS

137618-50-9Relevant articles and documents

Fumarate compounds, pharmaceutical compositions thereof, and methods of use

-

Page/Page column 59, (2017/01/26)

Fumarate compounds, pharmaceutical compositions comprising the fumarate compounds, and methods of using fumarate compounds and pharmaceutical compositions for treating neurodegenerative, inflammatory, and autoimmune disorders including multiple sclerosis, psoriasis, irritable bowel disorder, ulcerative colitis, arthritis, chronic obstructive pulmonary disease, asthma, Parkinson's disease, Huntington's disease, and amyotrophic lateral sclerosis are disclosed.

Selective monoalkylation of acyclic diols by means of dibutyltin oxide and fluoride salts

Nagashima,Ohno

, p. 1972 - 1982 (2007/10/02)

Fluoride anion was found to promote monoalkylation reaction of diols by the stannylene acetal method, and selective monoalkylation of various acyclic diols was accomplished in good yields under mild conditions by employing this new method. Functional groups such as carboxylic acid ester, carboxamide, carbamate, nitrile, alkyl chloride, and ether were not affected under the reaction conditions.

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