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141543-21-7

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141543-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141543-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,4 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 141543-21:
(8*1)+(7*4)+(6*1)+(5*5)+(4*4)+(3*3)+(2*2)+(1*1)=97
97 % 10 = 7
So 141543-21-7 is a valid CAS Registry Number.

141543-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name di(propan-2-yloxy)phosphoryl-(4-fluorophenyl)methanone

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:141543-21-7 SDS

141543-21-7Relevant articles and documents

Synthesis of 2-phosphonoheterocycles via base-promoted 5-endo cyclization

Bousbia, Ameni,Benkhoud, Mohamed Lamine,El-Ka?m, Laurent,Prévost, Sébastien

supporting information, (2021/01/14)

Herein, a synthesis of 2-phosphonodihydrofurans and 2-phosphonodihydropyrroles via 5-endo cyclization of O-and N-propargylated compounds is described. The reaction is promoted by potassium tert-butoxide and allows a fast access to interesting heterocycles which were easily converted into 2-arylated pyrroles under acidic conditions.

Palladium-catalyzed asymmetric hydrogenation of N-hydroxya-imino phosphonates using bronsted acid as activator: The first catalytic enantioselective approach to chiral N-hydroxy-aamino phosphonates

Goulioukina, Nataliya S.,Shergold, Ilya A.,Bondarenko, Grigorii N.,Ilyin, Mikhail M.,Davankov, Vadim A.,Beletskaya, Irina P.

supporting information, p. 2727 - 2733 (2013/01/15)

The enantioselective synthesis of ring-substituted [N-(hydroxy)amino] ACHTUNGTRENUNG(phenyl)methylphos- ACHTUNGTRENUNGphonic esters via asymmetric hydrogenation of the corresponding N-hydroxy-a-imino phosphonates with up to 90% ee was developed using cata

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