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354-43-8

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354-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 354-43-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 354-43:
(5*3)+(4*5)+(3*4)+(2*4)+(1*3)=58
58 % 10 = 8
So 354-43-8 is a valid CAS Registry Number.
InChI:InChI=1/C2H6F2NOP/c1-5(2)7(3,4)6/h1-2H3

354-43-8SDS

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 N,N-Dimethylphosphoroamidic difluoride

1.2 Other means of identification

Product number -
Other names dimethyl-amidophosphoryl fluoride

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:354-43-8 SDS

354-43-8Relevant articles and documents

Fluorinated phosphorus compounds: Part 1. The synthesis and reactions of some fluoroalkyl phosphoryl compounds

Timperley, Christopher M.,Bird, Michael,Broderick, John F.,Holden, Ian,Morton, Ian J.,Waters, Matthew J.

, p. 215 - 223 (2000)

Fluoroalkyl phosphorochloridates CF3CH2OP(O)Cl2 and (RFCH2O)2P(O)Cl (RF=CF3, C2F5) were prepared from phosphorus oxychloride, fluoroalcohols and triethylamine, but selective substitution was difficult. Phosphates (RFCH2O)2P(O)OR (RF=CF3, C2F5 and R=Me, Et, n-Pr, i-Pr) were isolated in yields of 38-84% from the reactions of the phosphorochloridates with alcohols and triethylamine. Success of the inverse reaction, i.e. ROP(O)Cl2 and RFCH2OH, depended on the R group (Me, Et) and the RF group (CF3, C2F5). The phosphates did not react with bromotrimethylsilane in chloroform. Addition of amines to CF3CH2OP(O)Cl2 or (CF3CH2O)2P(O)Cl gave phosphoramidates (RR′N)2P(O)OCH2CF3 or (CF3CH2O)2P(O)NRR′ (R and R′=H, Me, Et) in yields of 58-75%. The inverse reactions of Me2NP(O)Cl2 and (Me2N)2P(O)Cl with trifluoroethanol were slow, but were catalysed by 4-dimethylaminopyridine. Anhydrous hydrogen chloride split one of the P-N bonds of (Me2N)2P(O)OCH2CF3 to give Me2NP(O)Cl(OCH2CF3), but was without action on (CF3CH2O)2P(O)NMe2.

Fluorination of organochlorophosphorus compounds with alkali metal salts of perfluorinated complex anions. Part 2

Farooq, Omar

, p. 81 - 84 (2007/10/03)

Alkali metal salts of perfluorinated complex anions were used to fluorinate a few selected organochlorophosphorus compounds in the presence and absence of a multifunctional etheral solvent. Together with oxidative products, low to moderate yields of the desired monofluorinated products were obtained.

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