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2-Propenamide, N-[bis(4-butylphenyl)phenylmethyl]-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

632285-96-2

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632285-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 632285-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,2,2,8 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 632285-96:
(8*6)+(7*3)+(6*2)+(5*2)+(4*8)+(3*5)+(2*9)+(1*6)=162
162 % 10 = 2
So 632285-96-2 is a valid CAS Registry Number.

632285-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[bis(4-butylphenyl)-phenylmethyl]-2-methylprop-2-enamide

1.2 Other means of identification

Product number -
Other names N-[di(4-butylphenyl)phenylmethyl]methacrylamide

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:632285-96-2 SDS

632285-96-2Upstream product

632285-96-2Downstream Products

632285-96-2Relevant academic research and scientific papers

Stereospecific radical polymerization of N-triphenylmethylmethacrylamides leading to highly isotactic helical polymers

Hoshikawa, Naohiro,Hotta, Yuji,Okamoto, Yoshio

, p. 12380 - 12381 (2003)

N-Triphenylmethylmethacrylamide (TrMAM) and N-[di(4-butylphenyl)phenylmethyl]methacrylamide (DBuTrMAM) were polymerized using radical initiators. The polymer PTrMAM obtained from TrMAM was insoluble in the common solvents, but was dissolved in sulfuric acid to quantitatively give polymethacrylamide. The 1H NMR spectrum of PTrMAM in sulfuric acid-d2 indicated that the derived polymethacrylamide was nearly 100% isotactic. On the other hand, DBuTrMAM yielded the polymer PDBuTrMAM, which was soluble in THF and chloroform and whose NMR pattern in sulfuric acid-d2 was similar to that of PTrMAM. The polymerization of TrMAM and DBuTrMAM in an optically active solvent, (-)- or (+)-menthol, afforded the optically active polymers having a prevailing one-handed helical structure. The monomers were not solvolized in a methanol-chloroform mixture. TrMAM was not polymerized by anionic initiators. Copyright

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