Cas 352555-43-2,2-Thiophenecarboxylic acid, 3-amino-5-methyl-4-[[(2-phenylethyl)amino]carbonyl]-, ethyl ester

352555-43-2

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Basic information

Product Name: 2-Thiophenecarboxylic acid, 3-amino-5-methyl-4-[[(2-phenylethyl)amino]carbonyl]-, ethyl ester
Synonyms:
CAS NO:352555-43-2
Molecular Formula: C17H20N2O3S
Molecular Weight: 332.423
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-Thiophenecarboxylic acid, 3-amino-5-methyl-4-[[(2-phenylethyl)amino]carbonyl]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Thiophenecarboxylic acid, 3-amino-5-methyl-4-[[(2-phenylethyl)amino]carbonyl]-, ethyl ester(352555-43-2)
EPA Substance Registry System: 2-Thiophenecarboxylic acid, 3-amino-5-methyl-4-[[(2-phenylethyl)amino]carbonyl]-, ethyl ester(352555-43-2)

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: 352555-43-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 352555-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,5 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 352555-43:
(8*3)+(7*5)+(6*2)+(5*5)+(4*5)+(3*5)+(2*4)+(1*3)=142
142 % 10 = 2
So 352555-43-2 is a valid CAS Registry Number.

352555-43-2Upstream product

352555-43-2Downstream Products

352555-43-2Relevant academic research and scientific papers

Application of the Thorpe-Ziegler reaction for the synthesis of functionalized thiophenes, thienopyrimidines, and thienotriazines

Ryndina, S. A.,Kadushkin, A. V.,Solov'eva, N. P.,Granik, V. G.

, p. 854 - 859 (2007/10/03)

Approaches to the synthesis of 3-aminothiophene-2,4-dicarboxylic acid derivatives and to their conversions into thieno[3,4-d]pyrimidines, thieno[3,4-d]-1,2,3-triazines, and thieno[3,2-d]pyrimidines are developed.

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