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7148-06-3

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7148-06-3 Usage

Uses

N,N-Dimethylglycine methyl ester is used as a biochemical for proteomics research. It is also used as chemical and pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 7148-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7148-06:
(6*7)+(5*1)+(4*4)+(3*8)+(2*0)+(1*6)=93
93 % 10 = 3
So 7148-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c1-6(2)4-5(7)8-3/h4H2,1-3H3

7148-06-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L11897)  N,N-Dimethylglycine methyl ester, 98%   

  • 7148-06-3

  • 5g

  • 375.0CNY

  • Detail
  • Alfa Aesar

  • (L11897)  N,N-Dimethylglycine methyl ester, 98%   

  • 7148-06-3

  • 25g

  • 1491.0CNY

  • Detail

7148-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Dimethylglycine methyl ester

1.2 Other means of identification

Product number -
Other names methyl 2-(dimethylamino)acetate

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:7148-06-3 SDS

7148-06-3Relevant articles and documents

Substituent Effects on the Product Distribution in Diazo Amide Photochemistry. Role of Ground-State Conformational Populations

Tomioka, Hideo,Kondo, Masato,Izawa, Yasuji

, p. 1090 - 1094 (2007/10/02)

Effects of substituents on the photochemical processes of several α-diazo amides (1a-f) have been studied .Irradiation of 1b in ethyl ether and acetone afforded, in addition to a β-lactam, the reaction products with the solvents, ie., EtOCH2CONMe2 and 1,3-dioxolane, respectively, whereas similar irradiation of 1a in these solvents gave only intramolecular reaction products, ie., β- and γ-lactams.Displacement of oneof the alkyl groups on the amide nitrogen with a Ph group markedly changed its photochemical processes.Thus irradiations of 1c and 1d in MeOH gave oxindole almost exclusively.Introduction of an acetyl group on the diazo carbon also caused a change in the product distributions.Photolysis of 1e in methanol gave, for exaple, the Wolff rearrangement (WR) product of Me migration and a β-lactam, whereas similar irradiation of 1f afforded WR product and oxindole.The results are interpreted as indicating that the β-lactam, the oxindole, and the WR product are derived from the excited singlet state of s-Z form of the diazo amide itself, whereas that of s-E form dissociates nitrogen to generate singlet carbene, and that populations of each conformers in the ground state are important in determining the photochemical processes of the α-diazo amide.

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