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1038-94-4

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1038-94-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1038-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1038-94:
(6*1)+(5*0)+(4*3)+(3*8)+(2*9)+(1*4)=64
64 % 10 = 4
So 1038-94-4 is a valid CAS Registry Number.

1038-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-bromo-2,2-diphenylethenyl)-4-fluorobenzene

1.2 Other means of identification

Product number -
Other names 1-Brom-1-<4-fluor-phenyl>-2,2-diphenyl-aethylen

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:1038-94-4 SDS

1038-94-4Downstream Products

1038-94-4Relevant articles and documents

Phenanthrene Synthesis by Palladium-Catalyzed Benzannulation with o-Bromobenzyl Alcohols through Multiple Carbon-Carbon Bond Formations

Iwasaki, Masayuki,Araki, Yasuhiro,Nishihara, Yasushi

, p. 6242 - 6258 (2017)

A palladium-catalyzed benzannulation with o-bromobenzyl alcohols enabled the facile construction of phenanthrene skeletons via the sequential multiple carbon-carbon bond formations. A variety of multisubstituted phenanthrenes were synthesized by the reaction of (Z)-β-halostyrenes with o-bromobenzyl alcohols as well as by the three-component coupling of alkynes, aryl bromides, and o-bromobenzyl alcohols. The electron-deficient phosphine ligand played an important role to control the sequential oxidative addition of two different organic halides employed, which realized the selective formation of the desired phenanthrenes in good yields. This synthetic protocol was also applicable to the synthesis of the highly fused polycyclic aromatic hydrocarbons such as tetraphenes.

Synthetic antigonadotropins. IV. Bromotriphenylethylenes.

Fox,Gibas,Lee,Boris

, p. 415 - 416 (2007/10/15)

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