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32405-88-2

32405-88-2

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32405-88-2 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 96, p. 5937, 1974 DOI: 10.1021/ja00825a042

Check Digit Verification of cas no

The CAS Registry Mumber 32405-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,4,0 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32405-88:
(7*3)+(6*2)+(5*4)+(4*0)+(3*5)+(2*8)+(1*8)=92
92 % 10 = 2
So 32405-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H22NO3P/c1-3-13-15(12,14-4-2)11-10-8-6-5-7-9-10/h10H,3-9H2,1-2H3,(H,11,12)

32405-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-diethoxyphosphorylcyclohexanamine

1.2 Other means of identification

Product number -
Other names diethylcyclohexylamidophosphate

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:32405-88-2 SDS

32405-88-2Relevant articles and documents

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Wagner-Jauregg et al.

, p. 5202,5204 (1951)

-

Tf2O-Promoted Activating Strategy of Phosphate Analogues: Synthesis of Mixed Phosphates and Phosphinate

Huang, Hai,Ash, Jeffrey,Kang, Jun Yong

supporting information, p. 4938 - 4941 (2018/08/24)

A metal-, toxic chloride reagent-free activating strategy of various phosphates has been developed. This method enables the facile synthesis of functional phosphates such as alkyl phosphates, aza phosphates, thiophosphate, and mixed diaryl phosphates. A transient phosphorylpyridin-1-ium species in situ generated from phosphates with Tf2O/pyridine readily undergoes a substitution reaction with diverse nucleophiles to form versatile phosphate compounds.

Stereospecific aerobic oxidative dehydrocoupling of P(O)H bonds with amines catalyzed by copper

Zhou, Yongbo,Yang, Jia,Chen, Tieqiao,Yin, Shuang-Feng,Han, Daoqing,Han, Li-Biao

supporting information, p. 400 - 402 (2014/04/17)

Copper-catalyzed stereospecific oxidative dehydrocouplings of P(O)H bonds with amines under air took place effi-ciently at room temperature to afford the corresponding amidophosphorus compounds in high yields. Mechanistic studies showed that this dehydroc

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