Cas 1145668-35-4,ethyl 1-(3,4,5-trimethoxy)phenyl-9-n-butyl-β-carboline-3-carboxylic acid

1145668-35-4

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Basic information

Product Name: ethyl 1-(3,4,5-trimethoxy)phenyl-9-n-butyl-β-carboline-3-carboxylic acid
Synonyms: ethyl 1-(3,4,5-trimethoxy)phenyl-9-n-butyl-β-carboline-3-carboxylic acid
CAS NO:1145668-35-4
Molecular Formula:
Molecular Weight: 434.492
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: ethyl 1-(3,4,5-trimethoxy)phenyl-9-n-butyl-β-carboline-3-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 1-(3,4,5-trimethoxy)phenyl-9-n-butyl-β-carboline-3-carboxylic acid(1145668-35-4)
EPA Substance Registry System: ethyl 1-(3,4,5-trimethoxy)phenyl-9-n-butyl-β-carboline-3-carboxylic acid(1145668-35-4)

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: 1145668-35-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1145668-35-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,5,6,6 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1145668-35:
(9*1)+(8*1)+(7*4)+(6*5)+(5*6)+(4*6)+(3*8)+(2*3)+(1*5)=164
164 % 10 = 4
So 1145668-35-4 is a valid CAS Registry Number.

1145668-35-4Upstream product

1145668-33-2 ethyl 1-(3,4,5-trimethoxy)phenyl-9-n-butyl-β-carboline-3-carboxylate

1145668-35-4Downstream Products

1145668-35-4Relevant academic research and scientific papers

Synthesis and in vitro cytotoxic evaluation of novel 3,4,5-trimethoxyphenyl substituted β-carboline derivatives

Wu, Qifeng,Cao, Rihui,Feng, Manxiu,Guan, Xiangdong,Ma, Chunming,Liu, Jinbing,Song, Huacan,Peng, Wenlie

experimental part, p. 533 - 540 (2009/09/08)

To elucidate further our SARs' study on the chemistry and cytotoxic activity and probe the structural requirement for the potent antitumor activity of β-carbolines, a series of novel 1,9-disubstituted and 1,3,9-trisubstituted β-carboline derivatives were

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