Cas 138944-04-4,(3S,4S)-4-Dibenzylamino-3-hydroxy-2-methylene-5-phenyl-pentanoic acid methyl ester

138944-04-4

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Basic information

Product Name: (3S,4S)-4-Dibenzylamino-3-hydroxy-2-methylene-5-phenyl-pentanoic acid methyl ester
Synonyms:
CAS NO:138944-04-4
Molecular Formula:
Molecular Weight: 415.532
EINECS: N/A
Product Categories: N/A
Mol File: 138944-04-4.mol
Article Data: 2

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: (3S,4S)-4-Dibenzylamino-3-hydroxy-2-methylene-5-phenyl-pentanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S)-4-Dibenzylamino-3-hydroxy-2-methylene-5-phenyl-pentanoic acid methyl ester(138944-04-4)
EPA Substance Registry System: (3S,4S)-4-Dibenzylamino-3-hydroxy-2-methylene-5-phenyl-pentanoic acid methyl ester(138944-04-4)

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: 138944-04-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138944-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,9,4 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138944-04:
(8*1)+(7*3)+(6*8)+(5*9)+(4*4)+(3*4)+(2*0)+(1*4)=154
154 % 10 = 4
So 138944-04-4 is a valid CAS Registry Number.

138944-04-4Upstream product

138944-04-4Downstream Products

138944-04-4Relevant articles and documents

Addition of acrylamide to amino aldehydes to generate non-Baylis-Hillman adducts. Formation of novel N-acylhemiaminals

Bussolari, Jacqueline C.,Beers, Kimberly,Lalan, Praful,Murray, William V.,Gauthier, Diane,McDonnell, Patricia

, p. 787 - 788 (2007/10/03)

Aldol reactions of chiral aminoaldehydes and methylacrylate in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO) produces β-hydroxy methylbutenoates which can be utilized as psuedodipepetides. However, reaction of aminoaldehydes with acrylamide in the

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