Cas 213738-60-4,(E)-(5S,6R)-6-[2-(tert-Butyl-diphenyl-silanyloxymethyl)-oxazol-4-yl]-6-hydroxy-5-methyl-hex-3-enoic acid methyl ester

213738-60-4

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Basic information

Product Name: (E)-(5S,6R)-6-[2-(tert-Butyl-diphenyl-silanyloxymethyl)-oxazol-4-yl]-6-hydroxy-5-methyl-hex-3-enoic acid methyl ester
Synonyms:
CAS NO:213738-60-4
Molecular Formula:
Molecular Weight: 493.675
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: (E)-(5S,6R)-6-[2-(tert-Butyl-diphenyl-silanyloxymethyl)-oxazol-4-yl]-6-hydroxy-5-methyl-hex-3-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(5S,6R)-6-[2-(tert-Butyl-diphenyl-silanyloxymethyl)-oxazol-4-yl]-6-hydroxy-5-methyl-hex-3-enoic acid methyl ester(213738-60-4)
EPA Substance Registry System: (E)-(5S,6R)-6-[2-(tert-Butyl-diphenyl-silanyloxymethyl)-oxazol-4-yl]-6-hydroxy-5-methyl-hex-3-enoic acid methyl ester(213738-60-4)

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: 213738-60-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 213738-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,7,3 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 213738-60:
(8*2)+(7*1)+(6*3)+(5*7)+(4*3)+(3*8)+(2*6)+(1*0)=124
124 % 10 = 4
So 213738-60-4 is a valid CAS Registry Number.

213738-60-4Upstream product

136314-66-4 methyl (3S,4E)-3-(dimethylphenylsilyl)-4-hexenoate

213738-60-4Downstream Products

213738-60-4Relevant academic research and scientific papers

Studies directed toward the total synthesis of kabiramide C: Asymmetric synthesis of the C7-C19 fragment

Liu, Ping,Panek, James S.

, p. 6143 - 6146 (1998)

The synthesis of the C7-C19 tris-oxazole fragment 4 of kabiramide C via a BF3·OEt2 promoted condensation between dimethyl acetal 12 and (S)- silane 6 as the crucial synthetic step is described.

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