Cas 296229-49-7,(1S,2R)-2-{(S)-[Methyl-((R)-1-phenyl-ethyl)-amino]-phenyl-methyl}-1-phenyl-propane-1,3-diol

296229-49-7

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Basic information

Product Name: (1S,2R)-2-{(S)-[Methyl-((R)-1-phenyl-ethyl)-amino]-phenyl-methyl}-1-phenyl-propane-1,3-diol
Synonyms: (1S,2R)-2-{(S)-[Methyl-((R)-1-phenyl-ethyl)-amino]-phenyl-methyl}-1-phenyl-propane-1,3-diol
CAS NO:296229-49-7
Molecular Formula:
Molecular Weight: 375.511
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: (1S,2R)-2-{(S)-[Methyl-((R)-1-phenyl-ethyl)-amino]-phenyl-methyl}-1-phenyl-propane-1,3-diol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R)-2-{(S)-[Methyl-((R)-1-phenyl-ethyl)-amino]-phenyl-methyl}-1-phenyl-propane-1,3-diol(296229-49-7)
EPA Substance Registry System: (1S,2R)-2-{(S)-[Methyl-((R)-1-phenyl-ethyl)-amino]-phenyl-methyl}-1-phenyl-propane-1,3-diol(296229-49-7)

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: 296229-49-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 296229-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,2,2 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 296229-49:
(8*2)+(7*9)+(6*6)+(5*2)+(4*2)+(3*9)+(2*4)+(1*9)=177
177 % 10 = 7
So 296229-49-7 is a valid CAS Registry Number.

296229-49-7Upstream product

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296229-49-7Relevant academic research and scientific papers

Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-α-methylbenzyl amide

Davies, Stephen G.,Smethurst, Christian A.P.,Smith, Andrew D.,Smyth, G. Darren

, p. 2437 - 2441 (2000)

The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyright (C

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