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(1,3-di-tert-butyl-[1,3,2]diazaphosphinan-2-ylmethyl)-diethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60323-14-0

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60323-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60323-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,2 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60323-14:
(7*6)+(6*0)+(5*3)+(4*2)+(3*3)+(2*1)+(1*4)=80
80 % 10 = 0
So 60323-14-0 is a valid CAS Registry Number.

60323-14-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,3-di-tert-butyl-[1,3,2]diazaphosphinan-2-ylmethyl)-diethyl-amine

1.2 Other means of identification

Product number -
Other names 1,3-Di-tert.-butyl-2-[(diethylamino)methyl]hexahydro-1,3,2-diazaphosphorin

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:60323-14-0 SDS

60323-14-0Downstream Products

60323-14-0Relevant academic research and scientific papers

CYCLIC ORGANIC DERIVATIVES OF HYPOPHOSPHOROUS ACID

Nifantiev, E. E.,Sorokina, S. F.,Borisenko, A. A.,Zavalishina, A. I.,Vorobjeva, L. A.

, p. 3183 - 3194 (1981)

2-H-1,3,2-Dioxa-, dithia-, diaza- and oxaazaphosphorinanes have been prepared by reducing corresponding phosphorichloridates; spectral and chemical properties of these compounds have been studied.These compounds were considered as initial members of series when investigating the stereochemistry of heterocycles substituted at the phosphorus.The examination of 1H, 13C and 31P NMR spectra has shown that substitution of hydrogen at the phosphorus by axial halogen, alkyl, alkoxy and amido-groups is accompanied by shielding of 4,6-C atoms and deshielding of 4,6-axial protons; introduction of an axial Me group into γ-position to the P-H fragment causes a 30-40 ppm up-field shift of the resonance of the phosporus nucleus.

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