Cas 122040-29-3,2-[(1R,2S,5R)-1-((1S,3R)-4-Benzyloxy-1-benzyloxymethyl-3-hydroxy-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone

122040-29-3

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Basic information

Product Name: 2-[(1R,2S,5R)-1-((1S,3R)-4-Benzyloxy-1-benzyloxymethyl-3-hydroxy-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone
Synonyms: 2-[(1R,2S,5R)-1-((1S,3R)-4-Benzyloxy-1-benzyloxymethyl-3-hydroxy-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone
CAS NO:122040-29-3
Molecular Formula:
Molecular Weight: 572.785
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: 2-[(1R,2S,5R)-1-((1S,3R)-4-Benzyloxy-1-benzyloxymethyl-3-hydroxy-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(1R,2S,5R)-1-((1S,3R)-4-Benzyloxy-1-benzyloxymethyl-3-hydroxy-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone(122040-29-3)
EPA Substance Registry System: 2-[(1R,2S,5R)-1-((1S,3R)-4-Benzyloxy-1-benzyloxymethyl-3-hydroxy-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone(122040-29-3)

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: 122040-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122040-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,4 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122040-29:
(8*1)+(7*2)+(6*2)+(5*0)+(4*4)+(3*0)+(2*2)+(1*9)=63
63 % 10 = 3
So 122040-29-3 is a valid CAS Registry Number.

122040-29-3Upstream product

122040-29-3Downstream Products

122040-33-9 (2S,4R)-1,5-Bis-benzyloxy-4-methoxymethoxy-pentan-2-ol

122040-29-3Relevant academic research and scientific papers

ENANTIODIFFERENTIATING FUNCTIONALIZATION OF meso-1,3-DIOLS VIA SPIROACETALS DERIVED FROM l-MENTHONE

Harada, Toshiro,Sakamoto, Kazuhiko,Ikemura, Yoshifumi,Oku, Akira

, p. 3097 - 3100 (2007/10/02)

Enantiodifferentiating functionalization of meso-1,3-diols is realized by the utilization of titanium tetrachloride-promoted selective ring-cleavage reaction of spiroacetals derived from l-menthone.

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