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2612-87-5

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2612-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2612-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2612-87:
(6*2)+(5*6)+(4*1)+(3*2)+(2*8)+(1*7)=75
75 % 10 = 5
So 2612-87-5 is a valid CAS Registry Number.

2612-87-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-diphenylcyclopropyl)-trimethylsilane

1.2 Other means of identification

Product number -
Other names 2-Trimethylsilyl-1,1-diphenyl-cyclopropan

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:2612-87-5 SDS

2612-87-5Downstream Products

2612-87-5Relevant articles and documents

Cyclopropylidene Dianion Equivalent. Preparation of 1,1-Dilithio-2,2-diphenylcyclopropane

Oku, Akira,Ose, Yasuyoshi,Kamada, Tohru,Yoshida, Tomohiro

, p. 573 - 576 (1993)

The title compound was prepared by the treatment of corresponding 1,1-dibromocyclopropane with lithium naphthalene radical anion (Li-C10H8).Trapping of the dilithio compound by chlorotrimethylsilane provided evidence for its highly basic profile which can compete with silylation.

Nucleophilic Addition of Lithiated Phenyl Trimethylsilyl Sulfide to Activated Olefins. A Facile Synthesis of 2-(Functionally) Substituted Silylcyclopropanes

Schaumann, Ernst,Friese, Carsten,Spanka, Carsten

, p. 1035 - 1037 (2007/10/02)

The lithio derivative of phenyl trimethylsilylmethyl sulfide undergoes smooth addition to activated ethylene derivatives to afford trimethylsilylcyclopropanes, except for the addition to methyl 2-phenylpropenoate which leads to the formation of methyl 4-trimethylsilyl-2-phenyl-4-(phenylthio)butanoate.

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