Cas 143023-87-4,Acetamide, N-(4-chlorophenyl)-N-[2-(1-cyclohexen-1-yl)-2-methyl-1-thioxopropyl]-

143023-87-4

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Basic information

Product Name: Acetamide, N-(4-chlorophenyl)-N-[2-(1-cyclohexen-1-yl)-2-methyl-1-thioxopropyl]-
Synonyms:
CAS NO:143023-87-4
Molecular Formula: C18H22ClNOS
Molecular Weight: 335.898
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: Acetamide, N-(4-chlorophenyl)-N-[2-(1-cyclohexen-1-yl)-2-methyl-1-thioxopropyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, N-(4-chlorophenyl)-N-[2-(1-cyclohexen-1-yl)-2-methyl-1-thioxopropyl]-(143023-87-4)
EPA Substance Registry System: Acetamide, N-(4-chlorophenyl)-N-[2-(1-cyclohexen-1-yl)-2-methyl-1-thioxopropyl]-(143023-87-4)

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: 143023-87-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143023-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,0,2 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143023-87:
(8*1)+(7*4)+(6*3)+(5*0)+(4*2)+(3*3)+(2*8)+(1*7)=94
94 % 10 = 4
So 143023-87-4 is a valid CAS Registry Number.

143023-87-4Upstream product

75-36-5 acetyl chloride

143023-87-4Downstream Products

143023-93-2 N-(4-Chloro-phenyl)-N-(9,9-dimethyl-7-thia-tricyclo[4.3.0.0^1,8]non-8-yl)-acetamide

143023-87-4Relevant academic research and scientific papers

Photochemical Isomerisation of β,γ-Unsaturated Thioimides to 2-Thiabicyclopentanes

Sakamoto, Masami,Shigematsu, Ryoichi,Fujita, Tsutomu,Watanabe, Shoji

, p. 891 - 892 (2007/10/02)

Photolysis of N-acetyl-2,2-dimethylbut-3-enethioanilides 1 gave 1-(N-acetylanilino)-5,5-dimethyl-2-thiabicyclopentanes 2 in good yields via intramolecular cycloaddition of the thiocarbonyl group across the alkene; the corresponding amides w

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