Cas 1609930-35-9,methyl (1S,4aR,5S,8aR)-5-(2-{2-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)acetyl]furan-3-yl}ethyl)-1,4a-dimethyl-6-methylidenedecahydronaphthalene-1-carboxylate

1609930-35-9

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Product Name: methyl (1S,4aR,5S,8aR)-5-(2-{2-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)acetyl]furan-3-yl}ethyl)-1,4a-dimethyl-6-methylidenedecahydronaphthalene-1-carboxylate
Synonyms: methyl (1S,4aR,5S,8aR)-5-(2-{2-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)acetyl]furan-3-yl}ethyl)-1,4a-dimethyl-6-methylidenedecahydronaphthalene-1-carboxylate
CAS NO:1609930-35-9
Molecular Formula:
Molecular Weight: 529.679
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: methyl (1S,4aR,5S,8aR)-5-(2-{2-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)acetyl]furan-3-yl}ethyl)-1,4a-dimethyl-6-methylidenedecahydronaphthalene-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (1S,4aR,5S,8aR)-5-(2-{2-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)acetyl]furan-3-yl}ethyl)-1,4a-dimethyl-6-methylidenedecahydronaphthalene-1-carboxylate(1609930-35-9)
EPA Substance Registry System: methyl (1S,4aR,5S,8aR)-5-(2-{2-[2-(1-benzyl-1H-1,2,3-triazol-4-yl)acetyl]furan-3-yl}ethyl)-1,4a-dimethyl-6-methylidenedecahydronaphthalene-1-carboxylate(1609930-35-9)

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: 1609930-35-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609930-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,9,3 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1609930-35:
(9*1)+(8*6)+(7*0)+(6*9)+(5*9)+(4*3)+(3*0)+(2*3)+(1*5)=179
179 % 10 = 9
So 1609930-35-9 is a valid CAS Registry Number.

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1609930-35-9Relevant academic research and scientific papers

Synthetic transformation of higher terpenoids 31.* Synthesis of 1,2,3triazolyl-containing furan labdanoids and studies of their cytotoxic activity

Kharitonov,Shults,Shakirov,Pokrovskii,Pokrovskii,Tolstikov

, p. 2046 - 2055 (2014/07/07)

16-(1-R-1,2,3-Triazol-4-ylethyl), 16-(1-R-1,2,3-triazol-4-ylmethoxymethyl), and 16-{2-(1-R-1,2,3triazol4yl)-1-[(1-R-1,2,3-triazol-4-ylmethoxy)ethyl]} substituted deriva tives of methyl lambertianate were synthesized by 1,3-cycloaddition of labdanoid alkyn

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