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84208-33-3

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84208-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84208-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,0 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 84208-33:
(7*8)+(6*4)+(5*2)+(4*0)+(3*8)+(2*3)+(1*3)=123
123 % 10 = 3
So 84208-33-3 is a valid CAS Registry Number.

84208-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl)methyl 2-bromo-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names p-nitrobenzyl 2-bromo-2-methylpropionate

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:84208-33-3 SDS

84208-33-3Relevant articles and documents

On the pH sensitive optoelectronic properties of amphiphilic reduced graphene oxide via grafting of poly(dimethylaminoethyl methacrylate): A signature of p- and n-type doping

Kuila, Atanu,Maity, Nabasmita,Layek, Rama K.,Nandi, Arun K.

, p. 16039 - 16050 (2014)

Poly(N,N′-dimethylaminoethyl methacraylate) (PDMAEMA) functionalized reduced graphene oxide (rGO) is synthesized by atom transfer radical polymerization, followed by attachment to rGO via diazonium coupling. The rGO-PDMAEMA (RGP) is characterized by

1-SULFO-2-OXOAZETIDINE DERIVATIVES AND THEIR PRODUCTION

-

, (2011/08/10)

Disclosed are compounds of the general formula: wherein R1 is amino, an acylated amino or a protected amino group, X is hydrogen or methoxy, and R' is hydrogen, R or R4 wherein R is an organic residue attached to the azetidine ring through a carbon atom therein and R4 is azido, a halogen, an amino group which may optionally be acylated or a group of the formula wherein R5 is an organic residue and n is 0, 1 or 2, and pharmaceutically acceptable salts and esters thereof. The compounds have antimicrobial and/or Beta-lactamase-inhibitory activity and are of value as drugs for human beings and domesticated animals

Chemical modification of sulfazecin. Synthesis of 4-methoxycarbonyl-2-azetidinone-1-sulfonic acid derivatives

Kishimoto,Sendai,Tomimoto,Hashiguchi,Matsuo,Ochiai

, p. 2646 - 2659 (2007/10/02)

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