Cas 113408-06-3,Benzo[b]thiophene-3-carboxylic acid, 2-(benzoylamino)-7-hydroxy-4,6-dinitro-, ethyl ester

113408-06-3

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Basic information

Product Name: Benzo[b]thiophene-3-carboxylic acid, 2-(benzoylamino)-7-hydroxy-4,6-dinitro-, ethyl ester
Synonyms:
CAS NO:113408-06-3
Molecular Formula: C18H13N3O8S
Molecular Weight: 431.383
EINECS: N/A
Product Categories: N/A
Mol File: 113408-06-3.mol

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: Benzo[b]thiophene-3-carboxylic acid, 2-(benzoylamino)-7-hydroxy-4,6-dinitro-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzo[b]thiophene-3-carboxylic acid, 2-(benzoylamino)-7-hydroxy-4,6-dinitro-, ethyl ester(113408-06-3)
EPA Substance Registry System: Benzo[b]thiophene-3-carboxylic acid, 2-(benzoylamino)-7-hydroxy-4,6-dinitro-, ethyl ester(113408-06-3)

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: 113408-06-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113408-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,0 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113408-06:
(8*1)+(7*1)+(6*3)+(5*4)+(4*0)+(3*8)+(2*0)+(1*6)=83
83 % 10 = 3
So 113408-06-3 is a valid CAS Registry Number.

113408-06-3Upstream product

113407-94-6 2-Benzoylamino-6-bromo-7-hydroxy-benzo[b]thiophene-3-carboxylic acid ethyl ester

113408-06-3Downstream Products

113408-06-3Relevant academic research and scientific papers

SYNTHESIS OF DERIVATIVES OF 2-ACYLAMINO-7-OXYBENZOTHIOPHENE. BROMINATION AND NITRATION.

Grinev, A. N.,Kharizomenova, I. A.,Kapustina, M. V.,Sheinker, Yu. N.,Alekseeva, L. M.,Rubtsov, N. M.

, p. 384 - 386 (2007/10/02)

Bromination of 2-acylamino-3-ethoxycarbonyl-7-oxo-4,5,6,7-tetrahydrobenzothiophenes has been studied.This reaction affords 2-acylamino-6,6-dibromo-3-ethoxycarbonyl-7-oxo-4,5,6,7-tetrahydrobenzothiophene, which on dehydrobromination gives 6-bromo-7-o

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