Cas 116015-99-7,[4-(Benzyloxycarbonyl-{[(4-chloro-phenyl)-methyl-amino]-methyl}-amino)-phenyl]-carbamic acid benzyl ester

116015-99-7

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Basic information

Product Name: [4-(Benzyloxycarbonyl-{[(4-chloro-phenyl)-methyl-amino]-methyl}-amino)-phenyl]-carbamic acid benzyl ester
Synonyms:
CAS NO:116015-99-7
Molecular Formula:
Molecular Weight: 530.023
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: [4-(Benzyloxycarbonyl-{[(4-chloro-phenyl)-methyl-amino]-methyl}-amino)-phenyl]-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [4-(Benzyloxycarbonyl-{[(4-chloro-phenyl)-methyl-amino]-methyl}-amino)-phenyl]-carbamic acid benzyl ester(116015-99-7)
EPA Substance Registry System: [4-(Benzyloxycarbonyl-{[(4-chloro-phenyl)-methyl-amino]-methyl}-amino)-phenyl]-carbamic acid benzyl ester(116015-99-7)

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: 116015-99-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116015-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,1 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 116015-99:
(8*1)+(7*1)+(6*6)+(5*0)+(4*1)+(3*5)+(2*9)+(1*9)=97
97 % 10 = 7
So 116015-99-7 is a valid CAS Registry Number.

116015-99-7Upstream product

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116015-99-7Relevant academic research and scientific papers

Reactions of p-Benzoquinone Diimine Derivatives with N,N-Dimethylanilines

Miyagi, Yo,Maruyama, Kazuhiro,Kurokawa, Mitsunori,Yoshii, Ayumi

, p. 51 - 54 (2007/10/02)

N,N'-Bisalkoxycarbonyl-p-benzoquinone diimine underwent a thermal addition reaction with N,N-dimethylanilines to form an N-C bond between an imino group and an N-methyl group.Upon irradiation the reaction was accelerated.The reaction did not proceed with N-alkyl substituted anilines other than methyl.

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