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37011-83-9

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37011-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37011-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,1 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37011-83:
(7*3)+(6*7)+(5*0)+(4*1)+(3*1)+(2*8)+(1*3)=89
89 % 10 = 9
So 37011-83-9 is a valid CAS Registry Number.

37011-83-9SDS

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 1,4-dibromonaphthalene-d6

1.2 Other means of identification

Product number -
Other names 1,4-Dibrom-hexadeuterionaphthalin

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:37011-83-9 SDS

37011-83-9Upstream product

37011-83-9Downstream Products

37011-83-9Relevant articles and documents

Organic glass-forming materials: 1,3,5-Tris(naphthyl)benzene derivatives

Bonvallet, Paul A.,Breitkreuz, Caroline J.,Yong, Seol Kim,Todd, Eric M.,Traynor, Katherine,Fry, Charles G.,Ediger,McMahon, Robert J.

, p. 10051 - 10057 (2007)

(Chemical Equation Presented) The organic glass-forming materials 1,3-bis(1-naphthyl)-5-(2-naphthyl)benzene (2) and its partially deuterated analogue, 1,3-bis(1-naphthyl-d7)-5-(2-naphthyl)benzene (2-d 14), have been synthesized on a gram scale using Suzuki coupling reactions. Detailed spectroscopic studies afford complete NMR assignments ( 1H, 2H, 13C) for both compounds. Modest energy barriers for the interconversion of atropisomers (ca. 15 kcal/mol) result in a propensity for these materials to form supercooled liquids and glasses, rather than undergoing crystallization. The preparation of these materials enables detailed studies of physical properties of organic glasses and molecular diffusion in condensed phases.

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