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Silane, [3-(3-bromophenyl)propoxy](1,1-dimethylethyl)dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65537-55-5

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65537-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65537-55-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,3 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65537-55:
(7*6)+(6*5)+(5*5)+(4*3)+(3*7)+(2*5)+(1*5)=145
145 % 10 = 5
So 65537-55-5 is a valid CAS Registry Number.

65537-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-bromophenyl)propoxy-tert-butyl-dimethylsilane

1.2 Other means of identification

Product number -
Other names Silane,[3-(3-bromophenyl)propoxy](1,1-dimethylethyl)dimethyl

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:65537-55-5 SDS

65537-55-5Downstream Products

65537-55-5Relevant academic research and scientific papers

NiH-Catalyzed Reductive Relay Hydroalkylation: A Strategy for the Remote C(sp3)?H Alkylation of Alkenes

Zhou, Fang,Zhu, Jin,Zhang, Yao,Zhu, Shaolin

, p. 4058 - 4062 (2018/03/21)

The terminal-selective, remote C(sp3)?H alkylation of alkenes was achieved by a relay process combining NiH-catalyzed hydrometalation, chain walking, and alkylation. This method enables the construction of unfunctionalized C(sp3)?C(sp3) bonds under mild conditions from two simple feedstock chemicals, namely olefins and alkyl halides. The practical value of this transformation is further demonstrated by the large-scale and regioconvergent alkylation of isomeric mixtures of olefins at low catalyst loadings.

THERAPEUTIC SUBSTITUTED CYCLOPENTANES FOR REDUCING INTRAOCULAR PRESSURE

-

Page/Page column 49-50, (2009/03/07)

Disclosed herein are compounds having formula (I) wherein a dashed line represents the presence or absence of a bond; Y is an organic acid functional group, or an amide or ester thereof; or Y is hydroxymethyl or an ether thereof; or Y is a tetrazolyl func

Methylenecyclopentane derivatives

-

, (2008/06/13)

Methylenecyclopentane derivatives, for example STR1 wherein R2 is a blocking group such as tetrahydropyranyl, and a process for preparing them; said derivatives having utility as prostaglandin intermediates.

Inter-phenylene-PG amides

-

, (2008/06/13)

The present invention relates to novel amido, cycloamido, carbonylamido, sulfonylamido, and hydrazino derivatives of inter-phenylene-PG-type compounds. These novel derivatives produce surprisingly prolonged oral activity, particularly as anti-thrombotic agents, as compared to the previously known inter-phenylene-PG-type acids and esters.

4,5,6-Trinor-3,7-inter-m-phenylene prostaglandin F1α analogs

-

, (2008/06/13)

This invention is a group of 4,5,6-trinor-3,7-inter-m-phenylene prostaglandin-type compounds and processes for making them. These compounds are useful for a variety of pharmacological purposes, including hypotensive control and inhibition of platelet aggr

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