Cas 76345-61-4,2-(4-amino-3-nitrophenyl)amino-4-methylthiazole-5-carboxylic acid ethyl ester

76345-61-4

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Basic information

Product Name: 2-(4-amino-3-nitrophenyl)amino-4-methylthiazole-5-carboxylic acid ethyl ester
Synonyms: 2-(4-amino-3-nitrophenyl)amino-4-methylthiazole-5-carboxylic acid ethyl ester
CAS NO:76345-61-4
Molecular Formula:
Molecular Weight: 322.345
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: 2-(4-amino-3-nitrophenyl)amino-4-methylthiazole-5-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-amino-3-nitrophenyl)amino-4-methylthiazole-5-carboxylic acid ethyl ester(76345-61-4)
EPA Substance Registry System: 2-(4-amino-3-nitrophenyl)amino-4-methylthiazole-5-carboxylic acid ethyl ester(76345-61-4)

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: 76345-61-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76345-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,4 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76345-61:
(7*7)+(6*6)+(5*3)+(4*4)+(3*5)+(2*6)+(1*1)=144
144 % 10 = 4
So 76345-61-4 is a valid CAS Registry Number.

76345-61-4Upstream product

76345-61-4Downstream Products

76345-63-6 2-(3,4-diaminophenyl)amino-4-methylthiazole-5-carboxylic acid ethyl ester hydrochloride

76345-61-4Relevant academic research and scientific papers

Selective Functionalization in 2-Nitro-p-phenylenediamine : Part II - Synthesis of Derivatives of 5-(2-Thiazolylamino)benzimidazole 2-Carbamates

Rajappa, S.,Advani, B. G.,Sreenivasan, R.

, p. 536 - 538 (2007/10/02)

2-Nitro-p-phenylenediamine (1) reacts with methyl isothiocyanate to give N-methyl-thiourea (2).The unsubstituted thiourea (7) is obtained by similar addition of 1 to benzoyl isothiocyanate, followed by base-catalyzed removal of

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