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7682-06-6

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7682-06-6 Usage

General Description

2-(2-Methylprop-2-enoylamino)propanoic acid is a chemical compound with the molecular formula C8H13NO3. It is a derivative of propanoic acid and contains a 2-methylprop-2-enoylamino group. 2-(2-Methylprop-2-enoylamino)propanoic acid has potential applications in the pharmaceutical industry, as it may act as an intermediate in the synthesis of various drugs. Its properties and uses are still being researched, but it has the potential to contribute to the development of new pharmaceutical products.

Check Digit Verification of cas no

The CAS Registry Mumber 7682-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7682-06:
(6*7)+(5*6)+(4*8)+(3*2)+(2*0)+(1*6)=116
116 % 10 = 6
So 7682-06-6 is a valid CAS Registry Number.

7682-06-6SDS

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 N-Methacryloylalanine

1.2 Other means of identification

Product number -
Other names N-(methacryloyl)alanine

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:7682-06-6 SDS

7682-06-6Downstream Products

7682-06-6Relevant articles and documents

-

Iwakura,Y. et al.

, p. 2875 - 2878 (1966)

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Preparation and Enzymatic Hydrolysis of Polymers Anchoring Biphenyl-2-ol

Ishikawa, Tomomichi,Tanaka, Youji

, p. 1182 - 1185 (2007/10/02)

Polymers anchoring fungicidal biphenyl-2-ol(BPOL) were prepared by the polymerization and copolymerization of 2-biphenylyl methacrylate(BPMA) with various comonomers such as styrene, vinyl acetate, 2-hydroxyethyl methacrylate, N-methacryloylglycine, and N-methacryloyl-DL-alanine.The reactivity ratios of BPMA with the comonomers were evaluated.The α-chymotrypsin-catalyzed hydrolysis of the polymers was also studied.The release of BPOL from the polymers was represented by means of the Michaelis constant Km and the catalytic-rate constant kcat.The BPMA homopolymer gave higher Km and kcat values than the copolymers, and the copoly mers with a higher content of substrate units underwent cleavage more readily.It was found that the hydrolysis of the polymeric substrates is affected by the structure and character of the comonomer rather than the arrangement order of the repeating monomer units in the polymer sequence.

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