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101456-16-0

101456-16-0

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101456-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101456-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,4,5 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 101456-16:
(8*1)+(7*0)+(6*1)+(5*4)+(4*5)+(3*6)+(2*1)+(1*6)=80
80 % 10 = 0
So 101456-16-0 is a valid CAS Registry Number.

101456-16-0SDS

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 diphenoxyphosphoryl-(4-nitrophenyl)methanol

1.2 Other means of identification

Product number -
Other names diphenyl hydroxy(4-nitrophenyl)methylphosphonate

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:101456-16-0 SDS

101456-16-0Relevant articles and documents

Organocatalytic enantioselective hydrophosphonylation of aldehydes

Alegre-Requena, Juan V.,Marques-Lopez, Eugenia,Sanz Miguel, Pablo J.,Herrera, Raquel P.

, p. 1258 - 1264 (2014)

We report our results concerning the first squaramide-catalysed hydrophosphonylation of aldehydes. In all cases, the reactions proceeded smoothly and cleanly under mild reaction conditions rendering final α-hydroxy phosphonates in very good yields and hig

The Synthesis and Photochemistry of p-Dimethylamino-p'-nitrodiphenylethyne: a Push-Pull Acetylene

Gallagher, Michael J.,Noerdin, Hazli

, p. 997 - 1005 (2007/10/02)

The title compound (2) was prepared as a possible precursor to a push-pull cyclobutadiene, and its photochemistry examined under a wide range of conditions.The principal reaction observed was loss of a methyl group, and no evidence for bimolecular reactio

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