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1H-1,2,4-Diazaphosphole, 5-(1,1-dimethylethyl)-1,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93756-85-5

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93756-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93756-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93756-85:
(7*9)+(6*3)+(5*7)+(4*5)+(3*6)+(2*8)+(1*5)=175
175 % 10 = 5
So 93756-85-5 is a valid CAS Registry Number.

93756-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-tert-butyl-1,3-diphenyl-1,2,4-diazaphosphole

1.2 Other means of identification

Product number -
Other names 5-t-Butyl-1,3-diphenyl-1,2,4-diazaphosphole

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:93756-85-5 SDS

93756-85-5Downstream Products

93756-85-5Relevant academic research and scientific papers

Unusually Coordinated Phosphorus Compounds; 22. Cycloaddition Reactions of Nitrilium Betaines with a Stable Phosphaalkyne

Roesch, W.,Regitz, M.

, p. 689 - 693 (2007/10/02)

(2,2-Dimethylpropylidyne)phosphane (7) undergoes regiospecific -cycloaddition reactions with the arylnitrile oxides 2a-c to yield the 1,2,4-oxazaphospholes 8a-c.In the reaction of phosphaalkyne 7 with 2,2-dimethylpropanenitrile oxide (2d) the 1:2-adduct 10 is formed in addition to 8d.The reaction of 7 with the nitrile sulphide 12 produces the 1,2,4-thiazaphosphole 13.The 1H-1,2,4-diazaphospholes 18a-c are obtained from the reactions of 7 with the nitrile imines 17a-c; the regioisomers 21a and 21b have been detected by NMR spectroscopy.

1H-1,2,4 λ3-DIAZAPHOSPHOLE AUS 1,3,4-OXADIAZOLIUMSALZEN BZW. SYDNONEN

Maerkl, Gottfried,Pflaum, Siegfried

, p. 4415 - 4418 (2007/10/02)

1-Aryl(alkyl)-1,2,4λ3-diazaphospholes are obtained by the reaction of the title educts with tris-(trimethylsilyl)-phosphane resp. 1-chloro-2-phenyl-2-trimethylsilyl-1-phosphaethene

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