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3H-Indol-3-one, 1,2-dihydro-1-methyl-2,2-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81235-51-0

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81235-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81235-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,3 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81235-51:
(7*8)+(6*1)+(5*2)+(4*3)+(3*5)+(2*5)+(1*1)=110
110 % 10 = 0
So 81235-51-0 is a valid CAS Registry Number.

81235-51-0SDS

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-methyl-2,2-diphenyl-indolin-3-one

1.2 Other means of identification

Product number -
Other names 1-Methyl-2,2-diphenyl-indolin-3-on

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:81235-51-0 SDS

81235-51-0Relevant academic research and scientific papers

Alkylidenephosphoranes in heterocyclic synthesis: Reactivity of benzoxazinones with resonance-stabilized phosphorus ylides

Kamel, Azza A.,Abdou, Wafaa M.

, p. 1269 - 1273 (2007/12/27)

2H-3,1-Benzoxazine-2,4(1H)-dione and its N-methyl analogue react with alkylidenephosphoranes to give substituted quinolines and benzazepines as well as indanone and furan derivatives. Reaction mechanisms to explain the formation of products obtained are outlined. Georg Thieme Verlag Stuttgart.

Heterocyclic 8?-Systems, 16 - Elimination Reactions of 2-Alkoxy-3-hydroxyindolines

Beitzke, Bernhard,Schmidt, Richard R.

, p. 1726 - 1731 (2007/10/02)

Thermolysis of 2-ethoxy-3-hydroxyindolines 1a - f affords oxindoles 3a - f as main products and the corresponding 3-indolinones 2a - f as by-products.The reaction course via indole 2,3-oxide intermediates is discussed.For this reason rearrangement reactio

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