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108756-88-3

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108756-88-3 Usage

Chemical Properties

white powder

Check Digit Verification of cas no

The CAS Registry Mumber 108756-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,5 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 108756-88:
(8*1)+(7*0)+(6*8)+(5*7)+(4*5)+(3*6)+(2*8)+(1*8)=153
153 % 10 = 3
So 108756-88-3 is a valid CAS Registry Number.

108756-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name BORANE-DICYCLOHEXYLPHOSPHINE COMPLEX

1.2 Other means of identification

Product number -
Other names DICYCLOHEXYLPHOSPHINE BORANE COMPLEX

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:108756-88-3 SDS

108756-88-3Relevant articles and documents

A Diastereodivergent and Enantioselective Approach to syn- And anti-Diamines: Development of 2-Azatrienes for Cu-Catalyzed Reductive Couplings with Imines That Furnish Allylic Amines

Zhou, Pengfei,Shao, Xinxin,Malcolmson, Steven J.

, p. 13999 - 14008 (2021)

We introduce a new reagent class, 2-azatrienes, as a platform for catalytic enantioselective synthesis of allylic amines. Herein, we demonstrate their promise by a diastereodivergent synthesis of syn- and anti-1,2-diamines through their Cu-bis(phosphine)-catalyzed reductive couplings with imines. With Ph-BPE as the supporting ligand, anti-diamines are obtained (up to 91% yield, >20:1 dr, and >99:1 er), and with the rarely utilized t-Bu-BDPP, syn-diamines are generated (up to 76% yield, 1:>20 dr, and 97:3 er).

Sequential Pd0- and PdII-Catalyzed Cyclizations: Enantioselective Heck and Nucleopalladation Reactions

Arora, Ramon,Bajohr, Jonathan,Lautens, Mark,Torelli, Alexa,Whyte, Andrew

supporting information, p. 20231 - 20236 (2021/08/13)

An enantioselective consecutive cyclization/coupling process, catalyzed by palladium is reported. Stereoinduction arises from an enantioselective carbopalladation, generating an intermediate which promotes a nucleopalladation step. The dual cyclization se

The first IV group metal catalysts produced from these ligands and [...][...]

-

Paragraph 0182-0183, (2019/12/27)

Embodiments are directed to bis- and poly-phosphaguanidine compounds, and the metal-ligand complexes formed therefrom, wherein the metal complexes can be used as procatalysts in polyolefin polymerization. Formulas (I) (II) and (III).

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