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64929-62-0

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64929-62-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64929-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,2 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64929-62:
(7*6)+(6*4)+(5*9)+(4*2)+(3*9)+(2*6)+(1*2)=160
160 % 10 = 0
So 64929-62-0 is a valid CAS Registry Number.

64929-62-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(bromomethyl)-1-methoxy-2-propan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,4-(bromomethyl)-1-methoxy-2-(1-methylethyl)

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:64929-62-0 SDS

64929-62-0Relevant articles and documents

Syntheses and evaluation of multicaulin and miltirone-like compounds as antituberculosis agents

Burmao?lu, Serdar,Se?inti, Hatice,Mozio?lu, Erkan,G?ren, Ahmet C.,Altunda?, Ramazan,Se?en, Hasan

, p. 878 - 884 (2017/07/06)

Four multicaulin and miltirone-like phenanthrene derivatives were synthesised and evaluated as antituberculosis agents. The crucial step of the synthesis was Pschorr coupling of 4-(3-isopropyl-4-methoxyphenyl)-2-(2-aminophenyl)ethane (13) to give 2-isopro

Synthesis of aromatic diterpenes synthesis of 12-hydroxy-abieta-8,11,13-trien-3,7-dione

Burnell,Caron

, p. 127 - 132 (2007/10/02)

Model studies involving cationic cyclisation of suitable dienes have provided a synthesis of the title compound. Preparation of the dienes from available aromatic starting materials and the modification of the cyclised products are described.

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