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Stannane, dibromo(1-methylheptyl)phenyl-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96306-48-8

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96306-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96306-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,0 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96306-48:
(7*9)+(6*6)+(5*3)+(4*0)+(3*6)+(2*4)+(1*8)=148
148 % 10 = 8
So 96306-48-8 is a valid CAS Registry Number.

96306-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-2-octylphenyltin dibromide

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:96306-48-8 SDS

96306-48-8Upstream product

96306-48-8Downstream Products

96306-48-8Relevant academic research and scientific papers

Synthesis of optically active allyltin compounds and their application to enantioselective synthesis of secondary homoallyl alcohols

Otera, Junzo,Yoshinaga, Yukari,Yamaji, Takeshi,Yoshioka, Takakazu,Kawasaki, Yuzuru

, p. 1213 - 1218 (2008/10/08)

Three types of optically active allyltin compounds, R*2Sn(allyl)2 (R* = 2-phenylbutyl, 2-methylbutyl, and 3-phenylbutyl), R*R1Sn(allyl)2 (R* = 2-octyl or 2-phenylbutyl, R1 = phenyl), and R*R1R2Sn(allyl) (R* = 2-phenylbutyl, R1 = phenyl, R2 = methyl), have been synthesized. On the basis of 1H NMR spectra, a π-stacking interaction between the 2-phenylbutyl and the allyl groups is suggested. Optically active allyltin compounds thus obtained were subjected to reaction with aldehydes. Among various allyltin compounds, only diallylbis(2-phenylbutyl)tin exhibits good enantioselectivity. The reaction proceeds through addition of the allyl group on the re face of aldehydes. The mechanism can be accounted for on the basis of a π-stacking interaction between allyl and phenyl groups.

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