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1H-Phosphirene, 1-chloro-2,3-bis(1,1-dimethylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118398-72-4

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118398-72-4 Usage

Type of compound

Phosphorus-containing heterocyclic compound

Physical state

Colorless liquid

Odor

Pungent

Reactivity

Highly reactive due to the presence of the chlorine atom

Uses

Organic synthesis reagent for the preparation of various phosphorus-containing compounds, research and industrial applications for the synthesis of complex organic molecules

Handling precautions

Handle with care due to reactivity and potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 118398-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,9 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118398-72:
(8*1)+(7*1)+(6*8)+(5*3)+(4*9)+(3*8)+(2*7)+(1*2)=154
154 % 10 = 4
So 118398-72-4 is a valid CAS Registry Number.

118398-72-4SDS

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 2,3-ditert-butyl-1-chlorophosphirene

1.2 Other means of identification

Product number -
Other names 2,3-Di-tert-butyl-1-chlor-1H-phosphiren

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:118398-72-4 SDS

118398-72-4Downstream Products

118398-72-4Relevant academic research and scientific papers

1-Halogen-1H-phosphirene aus Phosphaalkinen und Halogencarbenen

Wagner, Oliver,Ehle, Michael,Birkel, Manfred,Hoffmann, Juergen,Regitz, Manfred

, p. 1207 - 1213 (2007/10/02)

Organophosphorus Compounds, 48. - 1-Halogen-1H-phosphirenes from Phosphaalkynes and Chlorocarbenes Halogen-substituted carbenes (7a-i), generated by thermolysis of diazirines (11a-i), add onto phosphaalkynes (8a-c) to form the title compounds (10a-l).Initially formed 2H-phosphirenes (9) could not be detected as their subsequent conversion to the 1H-isomers 10 by a 1,3-halogen shift is very fast.Hydrolysis of 10c,e,g-i and k yields vinylphosphonous acids (17a-e). 1-Chloro-1H-phosphirenes are transformed by nucleophilic substitution into fluoro (10a,c,e --> 19a-c), bromo (10c,e --> 20a,b), and iodo analogs (10c,e --> 21a,b) with the help of silver tetrafluoroborate, trimethylsilyl bromide, and trimethylsilyl iodide, respectively.A crystal structure analysis of 10c is reported.

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