Cas 881387-89-9,(4S,5R,6R)-4,6-Bis-((S)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane

881387-89-9

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Basic information

Product Name: (4S,5R,6R)-4,6-Bis-((S)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane
Synonyms: (4S,5R,6R)-4,6-Bis-((S)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane
CAS NO:881387-89-9
Molecular Formula:
Molecular Weight: 526.832
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: (4S,5R,6R)-4,6-Bis-((S)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R,6R)-4,6-Bis-((S)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane(881387-89-9)
EPA Substance Registry System: (4S,5R,6R)-4,6-Bis-((S)-2-benzyloxy-1-methyl-ethyl)-2,2-di-tert-butyl-5-methyl-[1,3,2]dioxasilinane(881387-89-9)

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: 881387-89-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 881387-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,3,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 881387-89:
(8*8)+(7*8)+(6*1)+(5*3)+(4*8)+(3*7)+(2*8)+(1*9)=219
219 % 10 = 9
So 881387-89-9 is a valid CAS Registry Number.

881387-89-9Upstream product

881387-89-9Downstream Products

881387-89-9Relevant academic research and scientific papers

Total synthesis of natural (+)-membrenone C and its 7-epimer

Yadav,Srinivas,Sathaiah

, p. 1603 - 1606 (2007/10/03)

Highly stereoselective asymmetric total syntheses of the polypropionate marine defense substance (+)-membrenone C and its 7-epimer have been achieved. Highlights of the strategy include the utilization of a desymmetrization technique to create five contig

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