Cas 1312920-72-1,(6-benzyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl 3-oxolup-20<sup>(29)</sup>-en-28-oate

1312920-72-1

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Basic information

Product Name: (6-benzyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl 3-oxolup-20⁽²⁹⁾-en-28-oate
Synonyms:
CAS NO:1312920-72-1
Molecular Formula:
Molecular Weight: 763.114
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: (6-benzyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl 3-oxolup-20⁽²⁹⁾-en-28-oate(CAS DataBase Reference)
NIST Chemistry Reference: (6-benzyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl 3-oxolup-20⁽²⁹⁾-en-28-oate(1312920-72-1)
EPA Substance Registry System: (6-benzyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-yl)methyl 3-oxolup-20⁽²⁹⁾-en-28-oate(1312920-72-1)

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: 1312920-72-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312920-72-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,9,2 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1312920-72:
(9*1)+(8*3)+(7*1)+(6*2)+(5*9)+(4*2)+(3*0)+(2*7)+(1*2)=121
121 % 10 = 1
So 1312920-72-1 is a valid CAS Registry Number.

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1312920-72-1Relevant academic research and scientific papers

Synthesis of conjugates of lupane triterpenoids with chromane antioxidants and in vitro study of their influence on the production of nitrogen monoxide and on the arginase activity in activated macrophages

Spivak,Khalitova,Bel'Skii,Ivanova,Shakurova,Bel'Skaya,Odinokov,Danilets,Ligacheva

, p. 2219 - 2229 (2010)

Conjugates of lupane triterpenoids (betulin and betulonic and betulinic acids) with synthetic analogs of α-tocopherol were obtained via ester bond formation and tested in vitro. Showing low cytotoxicity, some of them suppress nitrogen monoxide production

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