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88257-89-0

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88257-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88257-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,5 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88257-89:
(7*8)+(6*8)+(5*2)+(4*5)+(3*7)+(2*8)+(1*9)=180
180 % 10 = 0
So 88257-89-0 is a valid CAS Registry Number.

88257-89-0SDS

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 4,4-difluoro-1-phenylhexa-1,5-dien-3-ol

1.2 Other means of identification

Product number -
Other names 1,5-Hexadien-3-ol,4,4-difluoro-1-phenyl

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:88257-89-0 SDS

88257-89-0Relevant articles and documents

Synthesis of γ-fluoroalkylated allylic amines derivatives via palladium-catalyzed Overman rearrangement

Jiang, Xin-Yi,Chu, Lingling,Wang, Ruo-Wen,Qing, Feng-Ling

supporting information, p. 6853 - 6857,5 (2012/12/12)

A Pd-catalyzed Overman rearrangement of α-fluoroalkylated allylic trichloroacetimidates has been developed. This reaction allows for an efficient synthesis of γ-fluoroalkylated allylic amine derivatives with excellent regio- and stereo-selectivities under

An efficient and general route to gem-difluoromethylenated α,β-unsaturated δ-lactones: High enantioselective synthesis of gem-difluoromethylenated goniothalamins

You, Zheng-Wei,Jiang, Zhong-Xing,Wang, Bing-Lin,Qing, Feng-Ling

, p. 7261 - 7267 (2007/10/03)

An efficient and general strategy to gem-difluoromethylenated α,β-unsaturated δ-lactones in high yields from various aldehydes (including aliphatic, aromatic, α,β-unsaturated, and sterically hindered aldehydes) has been developed. This methodology was suc

The addition of dibromodifluoromethane to (trimethylsilyl)acetylene and transformation of the products

Qing, Feng-Ling,Wan, Dong-Peng

, p. 14189 - 14200 (2007/10/03)

Reaction of dibromodifluoromethane (1) with (trimethylsilyl)acetylene (2) initiated by ammonium persulfate/sodium formate ((NH4)2S2O8/HCO2Na) yield the addition-reduction product (3a), tribromide comp

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