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1,7-Distannacyclododecane, 1,1,7,7-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87518-35-2

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87518-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87518-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,1 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87518-35:
(7*8)+(6*7)+(5*5)+(4*1)+(3*8)+(2*3)+(1*5)=162
162 % 10 = 2
So 87518-35-2 is a valid CAS Registry Number.

87518-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,7,7-tetraphenyl-1,7-distannacyclododecane

1.2 Other means of identification

Product number -
Other names 1,7-Distannacyclododecane,1,1,7,7-tetraphenyl

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:87518-35-2 SDS

87518-35-2Downstream Products

87518-35-2Relevant academic research and scientific papers

Macrocycles containing tin. Syntheses of symmetrical macrocycles containing two or four diphenylstanna units

Azuma, Yutaka,Newcomb, Martin

, p. 9 - 14 (2008/10/08)

The syntheses of macrocycles containing two diphenylstanna moieties, c-[Ph2Sn(CH2)n-]2 (1, n = 4, 5, 6, 8, 10, 12), and four diphenylstanna moieties, c-[Ph2Sn(CH2)n-]4 (2, same n), are reported. α,ω-Bis-(bromomagnesio)alkanes reacted with Ph3SnCl to give α,ω-bis(triphenylstannyl)alkanes which upon treatment with HBr gave α,ω-bis(bromodiphenylstannyl)alkanes 4. Compounds 4 reacted with the corresponding chain length α,ω-bis(bromomagnesio)alkanes to give 1 and 2. Alternatively, good yields of 1 (n = 4, 5, 6, 8) were obtained by converting 4 to dilithium reagents 7 which were allowed to react with α,ω-dibromoalkanes. Good yields of 2 (n = 4-6) were obtained by first treating 4 with Cl(CH2)nMgBr to give dichlorides which were then allowed to react with 7 in a second step. Purifications of the macrocycles and several synthetic intermediates were effected by preparative reverse-phase chromatography. The macrocyclic products were characterized by NMR spectroscopy, molecular weight determinations, and elemental analyses.

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