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1H-Phosphole-2-carboxylic acid, 3,4-dimethyl-1-phenyl-1-sulfide is a complex organic compound with the molecular formula C13H13OPS. It is a derivative of 1H-phosphole, a heterocyclic compound containing phosphorus, carbon, and sulfur atoms. The structure of 1H-Phosphole-2-carboxylic acid, 3,4-dimethyl-1-phenyl-, 1-sulfide features a phosphole ring with a carboxylic acid group at the 2-position, a dimethyl group at the 3 and 4 positions, a phenyl group at the 1-position, and a sulfur atom bonded to the phosphorus atom. 1H-Phosphole-2-carboxylic acid, 3,4-dimethyl-1-phenyl-, 1-sulfide has potential applications in the synthesis of various organic compounds, pharmaceuticals, and materials science due to its unique structure and properties.

50485-90-0

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50485-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50485-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,8 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50485-90:
(7*5)+(6*0)+(5*4)+(4*8)+(3*5)+(2*9)+(1*0)=120
120 % 10 = 0
So 50485-90-0 is a valid CAS Registry Number.

50485-90-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-dimethyl-1-phenyl-1-sulfanylidene-1λ<sup>5</sup>-phosphole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Carboxy-3,4-dimethyl-1-phenylphospholsulfid

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:50485-90-0 SDS

50485-90-0Downstream Products

50485-90-0Relevant academic research and scientific papers

Preparation et proprietes de quelques sulfures de phospholes fonctionnels

Mathey

, p. 3127 - 3137 (2007/10/08)

tBuLi with 1-phenyl 3,4-dimethyl phosphole sulfide 1 in THF, gives a mesomeric anion 4. With aldehydes and ketones, this anion leads to methyl-substituted phospholes (6 and 9), 2-substituted phospholes (8) or 2-substituted 3-methylene phosphol 4-enes (5 and 7). With CO2 and CH3COOEt a 2-phosphole carboxylic acid 11 and a 2-acetyl phosphole 10 are obtained, respectively. The spectra of the 2-substituted phospholes are studied in some detail. Some of their chemical properties (dimerization, dissociation and tert-butylation) are also described.

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