Cas 147298-59-7,N-[2,2,2-Trichloro-1-(6-oxo-2-thioxo-3,6-dihydro-2H-pyrimidin-1-yl)-ethyl]-benzamide

147298-59-7

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Basic information

Product Name: N-[2,2,2-Trichloro-1-(6-oxo-2-thioxo-3,6-dihydro-2H-pyrimidin-1-yl)-ethyl]-benzamide
Synonyms: N-[2,2,2-Trichloro-1-(6-oxo-2-thioxo-3,6-dihydro-2H-pyrimidin-1-yl)-ethyl]-benzamide
CAS NO:147298-59-7
Molecular Formula:
Molecular Weight: 378.666
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: N-[2,2,2-Trichloro-1-(6-oxo-2-thioxo-3,6-dihydro-2H-pyrimidin-1-yl)-ethyl]-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2,2,2-Trichloro-1-(6-oxo-2-thioxo-3,6-dihydro-2H-pyrimidin-1-yl)-ethyl]-benzamide(147298-59-7)
EPA Substance Registry System: N-[2,2,2-Trichloro-1-(6-oxo-2-thioxo-3,6-dihydro-2H-pyrimidin-1-yl)-ethyl]-benzamide(147298-59-7)

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: 147298-59-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147298-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,9 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 147298-59:
(8*1)+(7*4)+(6*7)+(5*2)+(4*9)+(3*8)+(2*5)+(1*9)=167
167 % 10 = 7
So 147298-59-7 is a valid CAS Registry Number.

147298-59-7Upstream product

147298-59-7Downstream Products

136506-78-0 N(3)-<2,2,2-trichloro-1-benzoylamino-1-ethyl>uracil

147298-59-7Relevant academic research and scientific papers

REACTION OF 2-THIOURACIL WITH CARBOXYLIC ACID 1,2,2,2-TETRACHLOROETHYLAMIDES

Klyuchko, S. V.,Khutova, B. M.,Rozhenko, A. B.,Romanenko, E. A.,Vdovenko, S. I.,et al.

, p. 83 - 87 (1992)

Amidoalkylation of 2-thiouracil with 1,2,2,2-tetrachloroethylamides in the presence of triethylamine or sodium hydroxide gives products of S-, O-, and N-substitution, depending on the reaction conditions.

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