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methylenebis(diphenylphosphane)-borane(1:2) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24442-15-7

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24442-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24442-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,4 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24442-15:
(7*2)+(6*4)+(5*4)+(4*4)+(3*2)+(2*1)+(1*5)=87
87 % 10 = 7
So 24442-15-7 is a valid CAS Registry Number.

24442-15-7SDS

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 H2C(PPh2BH3)2

1.2 Other means of identification

Product number -
Other names methylenebis(diphenylphosphane)-borane(1:2)

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:24442-15-7 SDS

24442-15-7Relevant academic research and scientific papers

Calcium carbene complexes with boranophosphorano side-arms: CaC[P(Ph) 2BH3]2

Orzechowski, Lars,Jansen, Georg,Lutz, Martin,Harder, Sjoerd

, p. 2958 - 2964 (2009)

The ligand H2C(PPh2BH3)2 (4-H2) reacted with one or a half equivalent of (para-tBu-C 6H4CH2)2Ca·(THF)4 to form the calcium complexes Ca[HC(PPhsu

Catalyst-free alcoholysis of phosphane-boranes: a smooth, cheap, and efficient deprotection procedure

Van Overschelde, Michel,Vervecken, Elias,Modha, Sachin G.,Cogen, Simon,Van der Eycken, Erik,Van der Eycken, Johan

experimental part, p. 6410 - 6415 (2009/12/09)

Catalyst-free alcoholytic deprotection of borane-protected phosphorus compounds offers a smooth, efficient, and clean alternative to existing deprotection methods. In this paper we report our results on the general applicability of deprotecting phosphane-

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