Cas 916755-45-8,3-benzyloxymethyl-1-(2-bromo-6-methoxyquinolin-3-ylmethyl)-4-(1-ethylpropenyl)-1H-pyridin-2-one

916755-45-8

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Basic information

Product Name: 3-benzyloxymethyl-1-(2-bromo-6-methoxyquinolin-3-ylmethyl)-4-(1-ethylpropenyl)-1H-pyridin-2-one
Synonyms: 3-benzyloxymethyl-1-(2-bromo-6-methoxyquinolin-3-ylmethyl)-4-(1-ethylpropenyl)-1H-pyridin-2-one
CAS NO:916755-45-8
Molecular Formula:
Molecular Weight: 533.465
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-benzyloxymethyl-1-(2-bromo-6-methoxyquinolin-3-ylmethyl)-4-(1-ethylpropenyl)-1H-pyridin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-benzyloxymethyl-1-(2-bromo-6-methoxyquinolin-3-ylmethyl)-4-(1-ethylpropenyl)-1H-pyridin-2-one(916755-45-8)
EPA Substance Registry System: 3-benzyloxymethyl-1-(2-bromo-6-methoxyquinolin-3-ylmethyl)-4-(1-ethylpropenyl)-1H-pyridin-2-one(916755-45-8)

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: 916755-45-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 916755-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,7,5 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 916755-45:
(8*9)+(7*1)+(6*6)+(5*7)+(4*5)+(3*5)+(2*4)+(1*5)=198
198 % 10 = 8
So 916755-45-8 is a valid CAS Registry Number.

916755-45-8Upstream product

186668-50-8 1-{3-[(benzyloxy)methyl]-2-methoxy-4-pyridinyl}-1-propanone

916755-45-8Downstream Products

916755-46-9 8-benzyloxymethyl-7-(1-ethylpropenyl)-2-methoxy-11H-indolizino[1,2-b]quinolin-9-one

916755-45-8Relevant academic research and scientific papers

Synthesis of new camptothecin analogues with the E-lactone ring replaced by α,β-cyclohexenone

Bacherikov, Valeriy A.,Tsai, Tsong-Jen,Chang, Jang-Yang,Chou, Ting-Chao,Lee, Rong-Zau,Su, Tsann-Long

, p. 4490 - 4499 (2006)

The total synthesis of racemic camptothecin analogues 12a and 12b, in which the E-lactone ring has been replaced by an α,β-cyclohexenone ring and the ethyl and hydroxy substituents have been retained, was achieved by first preparing the ABCD fragments 31a

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