Cas 1207835-16-2,5-chloro-2-(2-methyl-1-phenylsulfonyl-1H-5-indolylamino)benzoic acid

1207835-16-2

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Basic information

Product Name: 5-chloro-2-(2-methyl-1-phenylsulfonyl-1H-5-indolylamino)benzoic acid
Synonyms: 5-chloro-2-(2-methyl-1-phenylsulfonyl-1H-5-indolylamino)benzoic acid
CAS NO:1207835-16-2
Molecular Formula:
Molecular Weight: 440.907
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-chloro-2-(2-methyl-1-phenylsulfonyl-1H-5-indolylamino)benzoic acid(CAS DataBase Reference)
NIST Chemistry Reference: 5-chloro-2-(2-methyl-1-phenylsulfonyl-1H-5-indolylamino)benzoic acid(1207835-16-2)
EPA Substance Registry System: 5-chloro-2-(2-methyl-1-phenylsulfonyl-1H-5-indolylamino)benzoic acid(1207835-16-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1207835-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1207835-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,8,3 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1207835-16:
(9*1)+(8*2)+(7*0)+(6*7)+(5*8)+(4*3)+(3*5)+(2*1)+(1*6)=142
142 % 10 = 2
So 1207835-16-2 is a valid CAS Registry Number.

1207835-16-2Upstream product

1207835-16-2Downstream Products

1207835-29-7 9,11-dichloro-2,methyl-3-phenylsulfonyl-3H-pyrrolo[3,2-a]acridine

1207835-16-2Relevant academic research and scientific papers

A short route to the synthesis of pyrroloacridines via Ullmann-Goldberg condensation

Meesala, Ramu,Nagarajan, Rajagopal

, p. 422 - 424 (2010)

A concise method for the preparation of pyrroloacridines was reported via CuI mediated Ullmann-Goldberg condensation of 5-amino-2-methylindoles and o-halobenzoic acid derivatives followed by cyclization with POCl3.

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