Cas 1449433-35-5,(Z)-benzyl 2-[5-(benzylamino)-4-(methylcarbamothioyl)-3-oxothien-2(3H)-ylidene]acetate

1449433-35-5

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Basic information

Product Name: (Z)-benzyl 2-[5-(benzylamino)-4-(methylcarbamothioyl)-3-oxothien-2(3H)-ylidene]acetate
Synonyms: (Z)-benzyl 2-[5-(benzylamino)-4-(methylcarbamothioyl)-3-oxothien-2(3H)-ylidene]acetate
CAS NO:1449433-35-5
Molecular Formula:
Molecular Weight: 424.544
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: (Z)-benzyl 2-[5-(benzylamino)-4-(methylcarbamothioyl)-3-oxothien-2(3H)-ylidene]acetate(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-benzyl 2-[5-(benzylamino)-4-(methylcarbamothioyl)-3-oxothien-2(3H)-ylidene]acetate(1449433-35-5)
EPA Substance Registry System: (Z)-benzyl 2-[5-(benzylamino)-4-(methylcarbamothioyl)-3-oxothien-2(3H)-ylidene]acetate(1449433-35-5)

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: 1449433-35-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449433-35-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,4,3 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1449433-35:
(9*1)+(8*4)+(7*4)+(6*9)+(5*4)+(4*3)+(3*3)+(2*3)+(1*5)=175
175 % 10 = 5
So 1449433-35-5 is a valid CAS Registry Number.

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1449433-35-5Relevant academic research and scientific papers

Influence of solvent and substituents on the reaction of N-alkylthioacetamides with dimethyl acetylenedicarboxylate: Synthesis of functionalized thiophenes containing an exocyclic double bond

Obydennov, Konstantin L.,Klimareva, Elena L.,Kosterina, Marya F.,Slepukhin, Pavel A.,Morzherin, Yury Yu.

, p. 4876 - 4879 (2013/09/02)

The reaction of thioacetamides with dimethyl acetylenedicarboxylate affords 3-oxothien-2-ylidene or 4-oxothiazol-2,5-ylidene derivatives based on the structure of the thioacetamides and the solvent employed. The structural features of the 3-oxothien-2-yli

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