Cas 1000774-83-3,methyl 2-(3,4-dichlorophenyl)-3-methyl-2H-isoindole-1-carboxylate

1000774-83-3

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Basic information

Product Name: methyl 2-(3,4-dichlorophenyl)-3-methyl-2H-isoindole-1-carboxylate
Synonyms: methyl 2-(3,4-dichlorophenyl)-3-methyl-2H-isoindole-1-carboxylate
CAS NO:1000774-83-3
Molecular Formula:
Molecular Weight: 334.202
EINECS: N/A
Product Categories: N/A
Mol File: 1000774-83-3.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: methyl 2-(3,4-dichlorophenyl)-3-methyl-2H-isoindole-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-(3,4-dichlorophenyl)-3-methyl-2H-isoindole-1-carboxylate(1000774-83-3)
EPA Substance Registry System: methyl 2-(3,4-dichlorophenyl)-3-methyl-2H-isoindole-1-carboxylate(1000774-83-3)

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: 1000774-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1000774-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,7,7 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1000774-83:
(9*1)+(8*0)+(7*0)+(6*0)+(5*7)+(4*7)+(3*4)+(2*8)+(1*3)=103
103 % 10 = 3
So 1000774-83-3 is a valid CAS Registry Number.

1000774-83-3Upstream product

1000774-83-3Downstream Products

1000774-83-3Relevant articles and documents

Sequential copper(I)-catalyzed reaction of amines with o-acetylenyl- substituted phenyldiazoacetates

Peng, Cheng,Cheng, Jiajia,Wang, Jianbo

scheme or table, p. 2359 - 2364 (2009/10/20)

A highly efficient, tetrakis(acetonitrile)-copper(I) hexafluorophosphate [Cu(MeCN)4PF6]-catalyzed tandem Cu(I)-carbene N-H insertion/Cu(I)-catalyzed hydroamination of alkynes, which leads to sequential formation of two C-N bonds to yield isoindole derivatives, has been developed.

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