Welcome to LookChem.com Sign In|Join Free
  • or
Stannane, tributyl[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

764661-20-3

Post Buying Request

764661-20-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

764661-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 764661-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,4,6,6 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 764661-20:
(8*7)+(7*6)+(6*4)+(5*6)+(4*6)+(3*1)+(2*2)+(1*0)=183
183 % 10 = 3
So 764661-20-3 is a valid CAS Registry Number.

764661-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tributyl-[(1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexyl]stannane

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:764661-20-3 SDS

764661-20-3Downstream Products

764661-20-3Relevant academic research and scientific papers

Pt-based chiral organotin modified heterogeneous catalysts for the enantioselective hydrogenation of 3,4-hexanedione

Vetere, Virginia,Faraoni, María B.,Podestá, Julio C.,Casella, Mónica L.

, p. 209 - 214 (2013/02/23)

In this paper we have studied the liquid-phase enantioselective hydrogenation of 3,4-hexanedione using Pt-based catalysts, modified with chiral organotin compounds derived from the (-)-menthyl group: (-)-Pt-MenSnBu 3 and (-)-Men3Sn-Sn-(-)-Men3. The organotin chiral modifiers were carefully synthesized and characterized in order to obtain optically pure compounds. The catalysts were prepared through a controlled surface reaction between the supported transition metal and the organometallic compound, using techniques derived from Surface Organometallic Chemistry on Metals (SOMC/M). The organobimetallic catalytic systems were found to be active and enantioselective in the hydrogenation of 3,4-hexanedione, yielding an enantiomeric excess of 25-27% for 4-hydroxy-3-hexanone.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 764661-20-3