Cas 1174151-06-4,methyl (R)-2-(benzyloxymethyl)-2-((2E,4E)-N-(4-methoxybenzyl)hexa-2,4-dienamido)-3-oxobutanoate

1174151-06-4

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Basic information

Product Name: methyl (R)-2-(benzyloxymethyl)-2-((2E,4E)-N-(4-methoxybenzyl)hexa-2,4-dienamido)-3-oxobutanoate
Synonyms: methyl (R)-2-(benzyloxymethyl)-2-((2E,4E)-N-(4-methoxybenzyl)hexa-2,4-dienamido)-3-oxobutanoate
CAS NO:1174151-06-4
Molecular Formula:
Molecular Weight: 465.546
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: methyl (R)-2-(benzyloxymethyl)-2-((2E,4E)-N-(4-methoxybenzyl)hexa-2,4-dienamido)-3-oxobutanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (R)-2-(benzyloxymethyl)-2-((2E,4E)-N-(4-methoxybenzyl)hexa-2,4-dienamido)-3-oxobutanoate(1174151-06-4)
EPA Substance Registry System: methyl (R)-2-(benzyloxymethyl)-2-((2E,4E)-N-(4-methoxybenzyl)hexa-2,4-dienamido)-3-oxobutanoate(1174151-06-4)

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: 1174151-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1174151-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,1,5 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1174151-06:
(9*1)+(8*1)+(7*7)+(6*4)+(5*1)+(4*5)+(3*1)+(2*0)+(1*6)=124
124 % 10 = 4
So 1174151-06-4 is a valid CAS Registry Number.

1174151-06-4Upstream product

1174151-06-4Downstream Products

1174151-07-5 C₂₇H₃₃NO₈

1174151-06-4Relevant academic research and scientific papers

Formal synthesis of salinosporamide A via NHC-catalyzed intramolecular lactonization

Struble, Justin R.,Bode, Jeffrey W.

experimental part, p. 4957 - 4967 (2009/11/30)

An N-heterocyclic carbene (NHC) catalyzed intramolecular lactonization to prepare densely functionalized bicyclic γ-lactam-γ-lactone adducts from enals is reported. This method has been applied to the formal synthesis of salinosporamide A, a potent 20S pr

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