Cas 1318802-53-7,1,1,1-trichloro-2-methylpropan-2-yl 2-benzyl-2-(4-methoxybenzamido)-3-oxo-3-(((S)-1-phenylethyl)amino)propanoate

1318802-53-7

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Basic information

Product Name: 1,1,1-trichloro-2-methylpropan-2-yl 2-benzyl-2-(4-methoxybenzamido)-3-oxo-3-(((S)-1-phenylethyl)amino)propanoate
Synonyms: 1,1,1-trichloro-2-methylpropan-2-yl 2-benzyl-2-(4-methoxybenzamido)-3-oxo-3-(((S)-1-phenylethyl)amino)propanoate
CAS NO:1318802-53-7
Molecular Formula:
Molecular Weight: 605.946
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: 1,1,1-trichloro-2-methylpropan-2-yl 2-benzyl-2-(4-methoxybenzamido)-3-oxo-3-(((S)-1-phenylethyl)amino)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: 1,1,1-trichloro-2-methylpropan-2-yl 2-benzyl-2-(4-methoxybenzamido)-3-oxo-3-(((S)-1-phenylethyl)amino)propanoate(1318802-53-7)
EPA Substance Registry System: 1,1,1-trichloro-2-methylpropan-2-yl 2-benzyl-2-(4-methoxybenzamido)-3-oxo-3-(((S)-1-phenylethyl)amino)propanoate(1318802-53-7)

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: 1318802-53-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1318802-53-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,8,8,0 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1318802-53:
(9*1)+(8*3)+(7*1)+(6*8)+(5*8)+(4*0)+(3*2)+(2*5)+(1*3)=147
147 % 10 = 7
So 1318802-53-7 is a valid CAS Registry Number.

1318802-53-7Upstream product

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1318802-53-7Relevant academic research and scientific papers

Catalytic enantioselective Steglich rearrangements using chiral N-heterocyclic carbenes

Campbell, Craig D.,Concellon, Carmen,Smith, Andrew D.

experimental part, p. 797 - 811 (2011/08/06)

The evaluation of a range of enantiomerically pure NHCs, prepared in situ from imidazolinium or triazolium salt precatalysts, to promote the catalytic enantioselective Steglich rearrangement of oxazolyl carbonates to their C-carboxyazlactones, is reported. Modest levels of enantioselectivity (up to 66% ee) are observed using oxazolidinone derived NHCs.

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