Cas 321658-35-9,3-Methoxy-5-methyl-naphthalene-1-carboxylic acid (S)-benzyloxycarbonyl-(1-methyl-cyclopropyl)-methyl ester

321658-35-9

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Basic information

Product Name: 3-Methoxy-5-methyl-naphthalene-1-carboxylic acid (S)-benzyloxycarbonyl-(1-methyl-cyclopropyl)-methyl ester
Synonyms: 3-Methoxy-5-methyl-naphthalene-1-carboxylic acid (S)-benzyloxycarbonyl-(1-methyl-cyclopropyl)-methyl ester
CAS NO:321658-35-9
Molecular Formula:
Molecular Weight: 418.489
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: 3-Methoxy-5-methyl-naphthalene-1-carboxylic acid (S)-benzyloxycarbonyl-(1-methyl-cyclopropyl)-methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-Methoxy-5-methyl-naphthalene-1-carboxylic acid (S)-benzyloxycarbonyl-(1-methyl-cyclopropyl)-methyl ester(321658-35-9)
EPA Substance Registry System: 3-Methoxy-5-methyl-naphthalene-1-carboxylic acid (S)-benzyloxycarbonyl-(1-methyl-cyclopropyl)-methyl ester(321658-35-9)

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: 321658-35-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 321658-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,6,5 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 321658-35:
(8*3)+(7*2)+(6*1)+(5*6)+(4*5)+(3*8)+(2*3)+(1*5)=129
129 % 10 = 9
So 321658-35-9 is a valid CAS Registry Number.

321658-35-9Upstream product

321658-35-9Downstream Products

321658-35-9Relevant academic research and scientific papers

A synthetic azinomycin analogue with demonstrated DNA cross-linking activity: Insights into the mechanism of action of this class of antitumor agent

Hartley, John A.,Hazrati, Ali,Kelland, Lloyd R.,Khanim, Ruzwana,Shipman, Michael,Suzenet, Franck,Walker, Louise F.

, p. 3467 - 3470 (2007/10/03)

An efficient synthesis of simplified azinomycin A and B analogues 1 and 2 (see picture) is described, and it is demonstrated that only 1, bearing both the epoxide and aziridine, induces interstrand cross-links in double-stranded DNA. Remarkably, a compoun

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