Cas 945674-96-4,(+)-{(1S,10R)-5-benzyloxy-1-(10-chloroethyl)-3-[(5-(1-methylpiperidin-4-yl-methoxy)-indol-2-yl)-carbonyl]-1,2-dihydro-3H-benz[e]indole}

945674-96-4

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Basic information

Product Name: (+)-{(1S,10R)-5-benzyloxy-1-(10-chloroethyl)-3-[(5-(1-methylpiperidin-4-yl-methoxy)-indol-2-yl)-carbonyl]-1,2-dihydro-3H-benz[e]indole}
Synonyms:
CAS NO:945674-96-4
Molecular Formula:
Molecular Weight: 608.18
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: (+)-{(1S,10R)-5-benzyloxy-1-(10-chloroethyl)-3-[(5-(1-methylpiperidin-4-yl-methoxy)-indol-2-yl)-carbonyl]-1,2-dihydro-3H-benz[e]indole}(CAS DataBase Reference)
NIST Chemistry Reference: (+)-{(1S,10R)-5-benzyloxy-1-(10-chloroethyl)-3-[(5-(1-methylpiperidin-4-yl-methoxy)-indol-2-yl)-carbonyl]-1,2-dihydro-3H-benz[e]indole}(945674-96-4)
EPA Substance Registry System: (+)-{(1S,10R)-5-benzyloxy-1-(10-chloroethyl)-3-[(5-(1-methylpiperidin-4-yl-methoxy)-indol-2-yl)-carbonyl]-1,2-dihydro-3H-benz[e]indole}(945674-96-4)

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: 945674-96-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945674-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,6,7 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 945674-96:
(8*9)+(7*4)+(6*5)+(5*6)+(4*7)+(3*4)+(2*9)+(1*6)=224
224 % 10 = 4
So 945674-96-4 is a valid CAS Registry Number.

945674-96-4Upstream product

916667-93-1 (+)-(1S,10R)-5-benzyloxy-3-(tert-butyloxycarbonyl)-1-(10-chloroethyl)-1,2-dihydro-3H-benz[e]indole

945674-96-4Downstream Products

945674-96-4Relevant academic research and scientific papers

Selective treatment of cancer: Synthesis, biological evaluation and structural elucidation of novel analogues of the antibiotic CC-1065 and the duocarmycins

Tietze, Lutz F.,Major, Felix,Schuberth, Ingrid,Spiegl, Dirk A.,Krewer, Birgit,Maksimenka, Katja,Bringmann, Gerhard,Magull, Joerg

, p. 4396 - 4409 (2008/02/08)

Novel diastereomerically pure β-D-galactosidic prodrugs (+)-12a-e of the cytotoxic antibiotics CC-1065 and the duocarmycins were prepared for an antibody directed enzyme prodrug therapy (ADEPT) using 4 as a substrate via a radical cyclization to give rac-

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