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Propanamide, 2-hydroxy-N-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51676-15-4

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51676-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51676-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51676-15:
(7*5)+(6*1)+(5*6)+(4*7)+(3*6)+(2*1)+(1*5)=124
124 % 10 = 4
So 51676-15-4 is a valid CAS Registry Number.

51676-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-N-methylpropanamide

1.2 Other means of identification

Product number -
Other names n-methyl-2-hydroxypropionamide

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:51676-15-4 SDS

51676-15-4Relevant academic research and scientific papers

Ru-catalyzed highly enantioselective hydrogenation of α-keto Weinreb amides

Zhao, Meng Meng,Li, Wan Fang,Ma, Xin,Fan, Wei Zheng,Tao, Xiao Ming,Li, Xiao Ming,Xie, Xiao Min,Zhang, Zhao Guo

, p. 342 - 348 (2013/07/26)

Asymmetric hydrogenation of α-keto Weinreb amides has been realized with [Ru((S)-Sunphos)(benzene)Cl]Cl as the catalyst and CeCl3· 7H2O as the additive. A series of enantiopure α-hydroxy Weinreb amides (up to 97% ee) have been obtained. Catalytic amount of CeCl 3·7H2O is essential for the high reactivity and enantioselectivity and the ratio of CeCl3·7H2O to [Ru((S)-Sunphos)(benzene)Cl]Cl plays an important role in the hydrogenation reaction.

Recovery of hydroxy acids from trash

-

, (2008/06/13)

This invention is a method for recovering hydroxy acid values from a poly(hydroxy acid) containing source, said method comprising, in order: (a) contacting the source with a solubilizing fluid in an amount of at least 1 mole of solubilizing fluid per mole of hydroxy acid equivalent present in the source, said solubilizing fluid selected from the group consisting of (1) water, (2) alcohols containing 1 to 6 carbon atoms, (3) mixtures of water and said alcohols, (4) amines of the formula HNR1R2, wherein R1 and R2 are independently selected from the group consisting of hydrogen and alkyl groups of 1-4 carbon atoms; (5) liquid media containing diamines of the formula H(R3)NR5N(R4)H, wherein R3 and R4 are independently selected from the group consisting of hydrogen and alkyl groups of 1-4 carbon atoms or are joined to form a heterocyclic ring, and R5 is alkylene of 2-12 carbon atoms or phenylene; and (6) mixtures of said amines and/or diamines with water and/or alcohols containing 1 to 6 carbon atoms.

Preparation of amide derivatives of hydroxy acids

-

, (2008/06/13)

Depolymerizing high molecular weight polyhydroxy acid by reacting with an amine to produce an amide derivative.

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