Structure

Methyl(2R,3S)-3-(tert-butoxycarbonylamino)-2-hydroxy-3-phenylpropionate

CAS
124605-42-1
Catalog Number
ACM124605421
Category
Other Products
Molecular Weight
295.33
Molecular Formula
C15H21NO5

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Specification

Synonyms
(2R,3S)-2-HYDROXY-3-(N-TERTBUTOXYCARBONYL) AMINO-3-PHENYL-METHYL PROPIONATE;(2r,3s)-n-tert-butoxycarbonyl-3-phenyl-isoserine methyl ester;BENZENEPROPANOIC ACID, BETA-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-ALPHA-HYDROXY-, METHYL ESTER;methyl (2r,3s)-3-(ter
IUPAC Name
methyl 2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoate
SMILES
CC(C)(C)OC(=O)NC(C1=CC=CC=C1)C(C(=O)OC)O
InChI Key
NCALQERIBRYGOK-UHFFFAOYSA-N
Density
1.170
Appearance
off-white crystal powde
EC Number
602-999-4
H-Bond Acceptor
5
H-Bond Donor
2

Upstream Synthesis Route 1

  • 140-10-3
  • 124605-42-1

Reference: [1]Tetrahedron Letters,1993,vol. 34,p. 6049 - 6052
[2]Heterocycles,1997,vol. 44,p. 305 - 318

Upstream Synthesis Route 2

  • 60512-85-8
  • 124605-42-1

Reference: [1]Journal of Organic Chemistry,1990,vol. 55,p. 1957 - 1959
[2]Heterocycles,1997,vol. 44,p. 305 - 318
[3]Tetrahedron Asymmetry,2000,vol. 11,p. 4485 - 4497

Downstream Synthesis Route 1

  • 124605-42-1
  • 196404-55-4

Reference: [1] Journal of Heterocyclic Chemistry, 2005, vol. 42, # 4, p. 679 - 684
[2] Patent: CN106632297, 2017, A,

Downstream Synthesis Route 2

  • 124605-42-1
  • 145514-62-1

Reference: [1] Chemical Communications, 2014, vol. 50, # 89, p. 13706 - 13709

Downstream Synthesis Route 3

  • 124605-42-1
  • 873914-63-7

Reference: [1]Journal of Heterocyclic Chemistry,2005,vol. 42,p. 679 - 684

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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