Cas 608537-16-2,(4RS)-6-[3-butenyl(phenylsulfonyl)amino]-4-hydroxymethyl-5-iodo-7-methoxy-1-phenylsulfonyl-1,2,3,4-tetrahydroquinoline

608537-16-2

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Basic information

Product Name: (4RS)-6-[3-butenyl(phenylsulfonyl)amino]-4-hydroxymethyl-5-iodo-7-methoxy-1-phenylsulfonyl-1,2,3,4-tetrahydroquinoline
Synonyms: (4RS)-6-[3-butenyl(phenylsulfonyl)amino]-4-hydroxymethyl-5-iodo-7-methoxy-1-phenylsulfonyl-1,2,3,4-tetrahydroquinoline
CAS NO:608537-16-2
Molecular Formula:
Molecular Weight: 668.574
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: (4RS)-6-[3-butenyl(phenylsulfonyl)amino]-4-hydroxymethyl-5-iodo-7-methoxy-1-phenylsulfonyl-1,2,3,4-tetrahydroquinoline(CAS DataBase Reference)
NIST Chemistry Reference: (4RS)-6-[3-butenyl(phenylsulfonyl)amino]-4-hydroxymethyl-5-iodo-7-methoxy-1-phenylsulfonyl-1,2,3,4-tetrahydroquinoline(608537-16-2)
EPA Substance Registry System: (4RS)-6-[3-butenyl(phenylsulfonyl)amino]-4-hydroxymethyl-5-iodo-7-methoxy-1-phenylsulfonyl-1,2,3,4-tetrahydroquinoline(608537-16-2)

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: 608537-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 608537-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,5,3 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 608537-16:
(8*6)+(7*0)+(6*8)+(5*5)+(4*3)+(3*7)+(2*1)+(1*6)=162
162 % 10 = 2
So 608537-16-2 is a valid CAS Registry Number.

608537-16-2Upstream product

608537-14-0 6-[3-butenyl(phenylsulfonyl)amino]-5-iodo-7-methoxy-4-methylene-1-phenylsulfonyl-1,2,3,4-tetrahydroquinoline

608537-16-2Downstream Products

608537-16-2Relevant academic research and scientific papers

Synthesis of ring size seco-analogs of the antitumor antibiotic CC-1065 by two consecutive transition metal-initiated transformations

Tietze, Lutz F.,Looft, Jan,Feuerstein, Tim

, p. 2749 - 2755 (2007/10/03)

Novel seco-analogs of CC-1065 1 were synthesized from comercially available nitroaniline by reduction, bromination, bisulfonation and bisallylation followed by reaction with tert-butyllithium, zirconocene and iodine. The obtained quinoline 6 was then transformed into 17 and 18, which, upon treatment with Pd0, led to 21 and 22, respectively. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

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