Cas 1174006-20-2,(2S,3S,E)-methyl 2-(tert-butoxycarbonylamino)-2-methyl-3-phenylhex-4-enoate

1174006-20-2

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Basic information

Product Name: (2S,3S,E)-methyl 2-(tert-butoxycarbonylamino)-2-methyl-3-phenylhex-4-enoate
Synonyms: (2S,3S,E)-methyl 2-(tert-butoxycarbonylamino)-2-methyl-3-phenylhex-4-enoate
CAS NO:1174006-20-2
Molecular Formula:
Molecular Weight: 333.428
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: (2S,3S,E)-methyl 2-(tert-butoxycarbonylamino)-2-methyl-3-phenylhex-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,E)-methyl 2-(tert-butoxycarbonylamino)-2-methyl-3-phenylhex-4-enoate(1174006-20-2)
EPA Substance Registry System: (2S,3S,E)-methyl 2-(tert-butoxycarbonylamino)-2-methyl-3-phenylhex-4-enoate(1174006-20-2)

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: 1174006-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1174006-20-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,0,0 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1174006-20:
(9*1)+(8*1)+(7*7)+(6*4)+(5*0)+(4*0)+(3*6)+(2*2)+(1*0)=112
112 % 10 = 2
So 1174006-20-2 is a valid CAS Registry Number.

1174006-20-2Upstream product

74-88-4 methyl iodide

1174006-20-2Downstream Products

1174006-27-9 (2S,3S)-methyl 2-(tert-butoxycarbonylamino)-2-methyl-4-oxo-3-phenylbutanoate

1174006-20-2Relevant academic research and scientific papers

Stereoselective synthesis of β-branched phenylalanine derivatives via chelate-claisen rearrangement

Quirin, Christian,Kazmaier, Uli

, p. 1725 - 1731 (2009)

Ester enolate Claisen rearrangement of chelated N-protected chiral amino acid cinnamyl esters results in the formation of substituted phenylalanine derivatives with unsaturated side chains in good yields and with a high degree of chirality transfer. Georg

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