Cas 766528-45-4,(3S,5S)-3-isopropyl-1,1-dimethoxy-8-methyl-7-methylene-nonan-5-ol

766528-45-4

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Basic information

Product Name: (3S,5S)-3-isopropyl-1,1-dimethoxy-8-methyl-7-methylene-nonan-5-ol
Synonyms: (3S,5S)-3-isopropyl-1,1-dimethoxy-8-methyl-7-methylene-nonan-5-ol
CAS NO:766528-45-4
Molecular Formula:
Molecular Weight: 272.428
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: (3S,5S)-3-isopropyl-1,1-dimethoxy-8-methyl-7-methylene-nonan-5-ol(CAS DataBase Reference)
NIST Chemistry Reference: (3S,5S)-3-isopropyl-1,1-dimethoxy-8-methyl-7-methylene-nonan-5-ol(766528-45-4)
EPA Substance Registry System: (3S,5S)-3-isopropyl-1,1-dimethoxy-8-methyl-7-methylene-nonan-5-ol(766528-45-4)

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: 766528-45-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 766528-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,6,5,2 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 766528-45:
(8*7)+(7*6)+(6*6)+(5*5)+(4*2)+(3*8)+(2*4)+(1*5)=204
204 % 10 = 4
So 766528-45-4 is a valid CAS Registry Number.

766528-45-4Upstream product

149-73-5 trimethyl orthoformate

766528-45-4Downstream Products

766528-45-4Relevant academic research and scientific papers

Desymmetrizing hydroformylation with the aid of a planar chiral catalyst-directing group

Breit, Bernhard,Breuninger, Daniel

, p. 10244 - 10245 (2007/10/03)

Desymmetrizing hydroformylation of bisalkenyl- and bisallylcarbinols could be achieved employing a chiral substrate-bound catalyst-directing group (o-DPPF) with excellent levels of diastereotopic alkene face and diastereotopic alkene group discrimination to give bifunctionalized chiral aldehydes in enantiomerically pure form. Copyright

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