Cas 1038622-94-4,[2-methyl-5-(4-methylacridin-9-ylamino)phenyl]carbamic acid 4-[bis(2-chloroethyl)amino]phenyl ester

1038622-94-4

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Basic information

Product Name: [2-methyl-5-(4-methylacridin-9-ylamino)phenyl]carbamic acid 4-[bis(2-chloroethyl)amino]phenyl ester
Synonyms: [2-methyl-5-(4-methylacridin-9-ylamino)phenyl]carbamic acid 4-[bis(2-chloroethyl)amino]phenyl ester
CAS NO:1038622-94-4
Molecular Formula:
Molecular Weight: 573.522
EINECS: N/A
Product Categories: N/A
Mol File: 1038622-94-4.mol
Article Data: 2

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: [2-methyl-5-(4-methylacridin-9-ylamino)phenyl]carbamic acid 4-[bis(2-chloroethyl)amino]phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [2-methyl-5-(4-methylacridin-9-ylamino)phenyl]carbamic acid 4-[bis(2-chloroethyl)amino]phenyl ester(1038622-94-4)
EPA Substance Registry System: [2-methyl-5-(4-methylacridin-9-ylamino)phenyl]carbamic acid 4-[bis(2-chloroethyl)amino]phenyl ester(1038622-94-4)

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: 1038622-94-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1038622-94-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,6,2 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1038622-94:
(9*1)+(8*0)+(7*3)+(6*8)+(5*6)+(4*2)+(3*2)+(2*9)+(1*4)=144
144 % 10 = 4
So 1038622-94-4 is a valid CAS Registry Number.

1038622-94-4Upstream product

156078-81-8 carbonic acid p-(bis-2-chloroethylamino)phenol ester-p-nitrophenyl ester

1038622-94-4Downstream Products

1038622-94-4Relevant articles and documents

Novel DNA-directed alkylating agents: Design, synthesis and potent antitumor effect of phenyl N-mustard-9-anilinoacridine conjugates via a carbamate or carbonate linker

Kapuriya, Naval,Kapuriya, Kalpana,Dong, Huajin,Zhang, Xiuguo,Chou, Ting-Chao,Chen, Yu-Ting,Lee, Te-Chang,Lee, Wen-Chuan,Tsai, Tung-Hu,Naliapara, Yogesh,Su, Tsann-Long

experimental part, p. 1264 - 1275 (2009/07/18)

A series of phenyl N-mustard-9-anilinoacridine conjugates via a carbamate or carbonate linker was synthesized for antitumor evaluation. The carbamate or carbonate linker is able to lower the reactivity of the phenyl N-mustard pharmacophore and thus, these

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