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Acetic acid, [[4-[[(1,1-dimethylethoxy)carbonyl]amino]phenyl]thio]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

447414-44-0

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447414-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 447414-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,7,4,1 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 447414-44:
(8*4)+(7*4)+(6*7)+(5*4)+(4*1)+(3*4)+(2*4)+(1*4)=150
150 % 10 = 0
So 447414-44-0 is a valid CAS Registry Number.

447414-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-(4-aminophenylthio)acetic acid

1.2 Other means of identification

Product number -
Other names 2-({4-[(tert-butoxycarbonyl)amino]phenyl}thio)acetic acid

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:447414-44-0 SDS

447414-44-0Relevant academic research and scientific papers

Searching for cyclin-dependent kinase inhibitors using a new variant of the cope elimination

Griffin, Roger J.,Henderson, Andrew,Curtin, Nicola J.,Echalier, Aude,Endicott, Jane A.,Hardcastle, Ian R.,Newell, David R.,Noble, Martin E. M.,Wang, Lan-Zhen,Golding, Bernard T.

, p. 6012 - 6013 (2007/10/03)

β-Piperidinoethylsulfides are oxidized by m-chloroperbenzoic acid to intermediates containing both N-oxide and sulfone functions. These undergo a Cope-type elimination to a vinylsulfone that can be captured by amines to afford β-aminoethylsulfones. When a

An unusual behaviour of N-(tert-butoxycarbonyl)- and N-pivaloyl-(methylthio)anilines in metallation reactions

Cabiddu, Maria Grazia,Cabiddu, Salvatore,Cadoni, Enzo,De Montis, Stefania,Fattuoni, Claudia,Melis, Stefana

, p. 2893 - 2897 (2007/10/03)

The metallation reaction of N-Boc-and N-Piv-(methylthio)anilines are here described. The results show that N-Boc derivatives are metallated only by superbases to give products substituted at the thiomethylic group. N-Piv derivatives show a different behaviour: ortho-derivative is metallated by both butyllithium and superbase at the thiomethylic carbon atom, while para-derivative is metallated in ortho to the N-Piv group by butyllithium and at the thiomethylic carbon atom by superbase. The meta-derivative is metallated only by superbase at the thiomethylic carbon atom.

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