Cas 119930-34-6,(E)-2-Acetyl-3-phenyl-5-trimethylsilanyl-pent-4-enoic acid methyl ester

119930-34-6

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Basic information

Product Name: (E)-2-Acetyl-3-phenyl-5-trimethylsilanyl-pent-4-enoic acid methyl ester
Synonyms: (E)-2-Acetyl-3-phenyl-5-trimethylsilanyl-pent-4-enoic acid methyl ester
CAS NO:119930-34-6
Molecular Formula:
Molecular Weight: 304.461
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)-2-Acetyl-3-phenyl-5-trimethylsilanyl-pent-4-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-Acetyl-3-phenyl-5-trimethylsilanyl-pent-4-enoic acid methyl ester(119930-34-6)
EPA Substance Registry System: (E)-2-Acetyl-3-phenyl-5-trimethylsilanyl-pent-4-enoic acid methyl ester(119930-34-6)

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: 119930-34-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119930-34-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,9,3 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 119930-34:
(8*1)+(7*1)+(6*9)+(5*9)+(4*3)+(3*0)+(2*3)+(1*4)=136
136 % 10 = 6
So 119930-34-6 is a valid CAS Registry Number.

119930-34-6Upstream product

119930-34-6Downstream Products

119930-34-6Relevant academic research and scientific papers

PALLADIUM-CATALYSED REGIOSELECTIVE REACTIONS OF SILYL-SUBSTITUTED ALLYLIC CARBONATES AND VINYL EPOXIDE

Tsuji, Jiro,Yuhara, Masami,Minato, Makoto,Yamada, Hisao,Sato, Fumie,Kobayashi, Yuichi

, p. 343 - 346 (1988)

Palladium-catalysed reaction of α-substituted γ-trimethylsilylated allylic carbonates with carbonucleophiles took place regioselectively at the α-carbon.Reaction of formic acid took place at γ-carbon to afford allylic silanes.Methyl acetoacetate attacked

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