Cas 1123535-01-2,(Z,Z)-methyl 2-[1,3-dibenzyl-1,3,4',5'-tetrahydro-4'-methyl-2'-(phenylimino)spiro[2H-benzo[d]imidazole-2,3'(2'H)-thiophen]-5'-ylidene]acetate

1123535-01-2

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Basic information

Product Name: (Z,Z)-methyl 2-[1,3-dibenzyl-1,3,4',5'-tetrahydro-4'-methyl-2'-(phenylimino)spiro[2H-benzo[d]imidazole-2,3'(2'H)-thiophen]-5'-ylidene]acetate
Synonyms: (Z,Z)-methyl 2-[1,3-dibenzyl-1,3,4',5'-tetrahydro-4'-methyl-2'-(phenylimino)spiro[2H-benzo[d]imidazole-2,3'(2'H)-thiophen]-5'-ylidene]acetate
CAS NO:1123535-01-2
Molecular Formula:
Molecular Weight: 545.705
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,Z)-methyl 2-[1,3-dibenzyl-1,3,4',5'-tetrahydro-4'-methyl-2'-(phenylimino)spiro[2H-benzo[d]imidazole-2,3'(2'H)-thiophen]-5'-ylidene]acetate(CAS DataBase Reference)
NIST Chemistry Reference: (Z,Z)-methyl 2-[1,3-dibenzyl-1,3,4',5'-tetrahydro-4'-methyl-2'-(phenylimino)spiro[2H-benzo[d]imidazole-2,3'(2'H)-thiophen]-5'-ylidene]acetate(1123535-01-2)
EPA Substance Registry System: (Z,Z)-methyl 2-[1,3-dibenzyl-1,3,4',5'-tetrahydro-4'-methyl-2'-(phenylimino)spiro[2H-benzo[d]imidazole-2,3'(2'H)-thiophen]-5'-ylidene]acetate(1123535-01-2)

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: 1123535-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1123535-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,3,5,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1123535-01:
(9*1)+(8*1)+(7*2)+(6*3)+(5*5)+(4*3)+(3*5)+(2*0)+(1*1)=102
102 % 10 = 2
So 1123535-01-2 is a valid CAS Registry Number.

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1123535-01-2Relevant academic research and scientific papers

An experimental and theoretical study on the interaction of N-heterocyclic carbene-derived 1,3-dipoles with methoxycarbonylallenes: Highly regio- and stereoselective [3+2]-cycloadditions controlled by the structures of N-heterocycles of 1,3-dipoles

Cheng, Ying,Wang, Bo,Wang, Xiao-Rong,Zhang, Jian-Hong,Fang, De-Cai

supporting information; experimental part, p. 2357 - 2367 (2009/07/25)

The reactions of N-heterocyclic carbene-derived 1,3-dipoles with methoxycarbonylallenes were studied systematically by means of experimental and theoretical approach. The regioselectivity of [3+2]-cycloaddition of 1,3-dipoles toward the ester-substituted

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