Cas 143647-69-2,1H-Isoindol-1-one, 3-[2-(4-bromophenyl)-2-chloroethenyl]-2,3-dihydro-3-hydroxy-2-methyl-

143647-69-2

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Basic information

Product Name: 1H-Isoindol-1-one, 3-[2-(4-bromophenyl)-2-chloroethenyl]-2,3-dihydro-3-hydroxy-2-methyl-
Synonyms:
CAS NO:143647-69-2
Molecular Formula: C17H13BrClNO2
Molecular Weight: 378.653
EINECS: N/A
Product Categories: N/A
Mol File: 143647-69-2.mol
Article Data: 1

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: 1H-Isoindol-1-one, 3-[2-(4-bromophenyl)-2-chloroethenyl]-2,3-dihydro-3-hydroxy-2-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Isoindol-1-one, 3-[2-(4-bromophenyl)-2-chloroethenyl]-2,3-dihydro-3-hydroxy-2-methyl-(143647-69-2)
EPA Substance Registry System: 1H-Isoindol-1-one, 3-[2-(4-bromophenyl)-2-chloroethenyl]-2,3-dihydro-3-hydroxy-2-methyl-(143647-69-2)

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: 143647-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143647-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,4 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 143647-69:
(8*1)+(7*4)+(6*3)+(5*6)+(4*4)+(3*7)+(2*6)+(1*9)=142
142 % 10 = 2
So 143647-69-2 is a valid CAS Registry Number.

143647-69-2Upstream product

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143647-69-2Relevant articles and documents

The Mayer-Shuster Rearrangement and Hydrohalide Addition of 3-Alkynyl-3-hydroxy-1H-isoindol-1-ones

Omar, Enouri A.,Tu, Chi,Wigal, Carl T.,Braun, Loren L.

, p. 947 - 951 (2007/10/02)

Treatment of N-methyl and N-phenylphthalimide with appropiate lithium acetylides in tetrahydrofuran obtained the acetylenic alcohols 2a through 2h.These compounds when subjected to mildly acidic hydrolysis conditions in aqueous organic solvents, underwent

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