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62785-53-9

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62785-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62785-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62785-53:
(7*6)+(6*2)+(5*7)+(4*8)+(3*5)+(2*5)+(1*3)=149
149 % 10 = 9
So 62785-53-9 is a valid CAS Registry Number.

62785-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-di-tert-butyl-2,2,2-triphenyl-2λ5-benzo[1,3,2]dioxaphosphole

1.2 Other means of identification

Product number -
Other names 4,6-Di-tert-butyl-2,2,2-triphenyl-1,3-dioxa-2λ5-phospha-indan

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:62785-53-9 SDS

62785-53-9Downstream Products

62785-53-9Relevant articles and documents

Reactions of asymmetrically substituted o-quinones: 3,5-di-tert-butyl-1,2-benzoquinone with triphenyl-phosphine, -arsine, -stibine, their oxides and trialkyl phosphates

Abdou, Wafaa M.,Elkhoshneih, Yehia O.,Kamel, Azza A.

, p. 75 - 88 (1997)

The entitled quinone 4 reacts with triphenylphosphine (3a) and triphenylarsine (3b) to give the cyclic products 12a and 12b, respectively. The same quinone reacts with triphenylstibine (3c) to yield the stibine-methylene 17. The reaction of oxides of 3a-c (5a-c) and trialkyl phosphates 6a-c with the same quinone 4 affords hydrogen bonded complexes 13a-c and o-quinol monophosphates 23a-c, respectively. In both cases compound 22 is the other product. Possible reaction mechanisms are proposed to explain the formation of the new adducts.

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