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29265-79-0

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29265-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29265-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29265-79:
(7*2)+(6*9)+(5*2)+(4*6)+(3*5)+(2*7)+(1*9)=140
140 % 10 = 0
So 29265-79-0 is a valid CAS Registry Number.

29265-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-3-(1-phenylethenyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:29265-79-0 SDS

29265-79-0Relevant articles and documents

Preparation and morphology of ring-shaped polystyrene-block-polyisoprenes

Takano, Atsushi,Kadoi, Osamu,Hirahara, Kazuhiro,Kawahara, Seiichi,Isono, Yoshinobu,Suzuki, Jiro,Matsushita, Yushu

, p. 3045 - 3050 (2003)

Three polystyrene-block-polyisoprene-block-polystyrenes (SIS) with different compositions were prepared and cyclized by the coupling reaction between two end groups on the same molecules. Ring-shaped polystyrene-block-polyisoprenes (SI) were isolated from

Metal-free oxidative cross-coupling of diazirines with arylboronic acids

Wu, Guojiao,Zhao, Xia,Ji, Wenzhi,Zhang, Yan,Wang, Jianbo

, p. 1961 - 1963 (2016/02/05)

We report herein a metal-free cross-coupling of diazirines with arylboronic acids under oxidative conditions. The reaction affords a series of substituted olefins. It is proposed that the interaction between the nitrogen on diazirine with arylboronic acid plays a key role in this transformation.

4,5-DIHYDRO-OXAZOL-2-YL AMINE DERIVATIVES

-

Page/Page column 9, (2009/09/05)

The present invention relates to a compounds of formula I wherein R1, R1′, R2, R3, R4, X, Ar, and m are as defined in the specification and claims and pharmaceutically active acid addition salts thereof. Compounds of the invention have Asp2 (β-secretase, BACE 1 or Memapsin-2) inhibitory activity and are useful for the treatment of diseases characterized by elevated β-amyloid levels or β-amyloid deposits, particularly Alzheimer's disease.

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