Cas 863492-82-4,Butanoic acid, 4-azido-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methyl-, tris(1-methylethyl)silyl ester, (2S,3R)-

863492-82-4

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Basic information

Product Name: Butanoic acid, 4-azido-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methyl-, tris(1-methylethyl)silyl ester, (2S,3R)-
Synonyms:
CAS NO:863492-82-4
Molecular Formula: C20H43N3O3Si2
Molecular Weight: 429.751
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: Butanoic acid, 4-azido-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methyl-, tris(1-methylethyl)silyl ester, (2S,3R)-(CAS DataBase Reference)
NIST Chemistry Reference: Butanoic acid, 4-azido-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methyl-, tris(1-methylethyl)silyl ester, (2S,3R)-(863492-82-4)
EPA Substance Registry System: Butanoic acid, 4-azido-3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-methyl-, tris(1-methylethyl)silyl ester, (2S,3R)-(863492-82-4)

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: 863492-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 863492-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,4,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 863492-82:
(8*8)+(7*6)+(6*3)+(5*4)+(4*9)+(3*2)+(2*8)+(1*2)=204
204 % 10 = 4
So 863492-82-4 is a valid CAS Registry Number.

863492-82-4Upstream product

863492-82-4Downstream Products

115566-02-4 bistramide A

863492-82-4Relevant academic research and scientific papers

Stereoselective total synthesis of bistramide A

Yadav,Chetia, Lakshindra

, p. 4587 - 4589 (2007)

(Chemical Equation Presented) A highly stereoselective and convergent total synthesis of bistramide A is described. The salient feature of this synthesis is the construction of the spiroketal subunit by hydrolysis of dialkylated tosylmethyl isocyanide derivative derived via alkylation of TosMIC with suitably substituted halohydrin derivatives.

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