Cas 1255313-45-1,6-[1-hydroxy-2-(4-nitrophenyl)ethyl]-3-methylbenzo[d]thiazol-2(3H)-one

1255313-45-1

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Basic information

Product Name: 6-[1-hydroxy-2-(4-nitrophenyl)ethyl]-3-methylbenzo[d]thiazol-2(3H)-one
Synonyms: 6-[1-hydroxy-2-(4-nitrophenyl)ethyl]-3-methylbenzo[d]thiazol-2(3H)-one
CAS NO:1255313-45-1
Molecular Formula:
Molecular Weight: 330.364
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: 6-[1-hydroxy-2-(4-nitrophenyl)ethyl]-3-methylbenzo[d]thiazol-2(3H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 6-[1-hydroxy-2-(4-nitrophenyl)ethyl]-3-methylbenzo[d]thiazol-2(3H)-one(1255313-45-1)
EPA Substance Registry System: 6-[1-hydroxy-2-(4-nitrophenyl)ethyl]-3-methylbenzo[d]thiazol-2(3H)-one(1255313-45-1)

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: 1255313-45-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1255313-45-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,3,1 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1255313-45:
(9*1)+(8*2)+(7*5)+(6*5)+(5*3)+(4*1)+(3*3)+(2*4)+(1*5)=131
131 % 10 = 1
So 1255313-45-1 is a valid CAS Registry Number.

1255313-45-1Upstream product

1255313-45-1Downstream Products

1255313-45-1Relevant academic research and scientific papers

Original TDAE reactivity in benzoxa- and benzothiazolone series

Aida R. Nadji-Boukrouche,Khoumeri, Omar,Terme, Thierry,Liacha, Messaoud,Vanellec, Patrice

experimental part, p. 358 - 370 (2010/12/25)

We present herein an extension of the TDAE strategy using original heterocyclic carbaldehyde as electrophiles. We also evaluate the influence of the presence of nitro group on the reactivity. The TDAE-initiated reactions of various halomethyl and gem-diha

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