Boc-L-alaninal

Suppliers

Names

[ CAS No. ]:
79069-50-4

[ Name ]:
Boc-L-alaninal

[Synonym ]:
tert-Butyl [(2S)-1-oxopropan-2-yl]carbamate
Boc-L-alanine aldehyde
(S)-tert-Butyl (1-oxopropan-2-yl)carbamate
Carbamic acid, N-[(1S)-1-methyl-2-oxoethyl]-, 1,1-dimethylethyl ester
Boc-alaninal
Boc-Ala-Aldehyde
2-Methyl-2-propanyl (1-oxo-2-propanyl)carbamate
N-T-BOC-L-ALANINAL
2-Methyl-2-propanyl [(2S)-1-oxo-2-propanyl]carbamate
N-Boc-L-alaninal
Boc-L-alaninal
boc-L-alanine
Carbamic acid, N-(1-methyl-2-oxoethyl)-, 1,1-dimethylethyl ester
Boc-Ala-H

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
248.5±23.0 °C at 760 mmHg

[ Melting Point ]:
89 °C

[ Molecular Formula ]:
C8H15NO3

[ Molecular Weight ]:
173.210

[ Flash Point ]:
104.1±22.6 °C

[ Exact Mass ]:
173.105194

[ PSA ]:
55.40000

[ LogP ]:
1.23

[ Appearance of Characters ]:
Powder | White to yellow

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.436

[ Storage condition ]:
−20°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Precursor & DownStream

Precursor

  • (R)-TERT-BUTYL1-(METHOXY(METHYL)AMINO)-1-OXOPROPAN-2-YLCARBAMATE
  • Boc-Ala-Ome
  • N-Boc-L-alaninol
  • oxalic acid chloride
  • γ-(p-Anisidino)-buttersaeureaethylester
  • boc-l-alanine-nca
  • Carbamic acid, [(1S)-2-fluoro-1-methyl-2-oxoethyl]-, 1,1-dimethylethyl ester
  • Oxalyl chloride
  • Carbamic acid, [(1S)-1-methyl-2-propenyl]-, 1,1-dimethylethyl ester (9CI)

DownStream

  • 2-Pentenoic Acid, 4-[[)1,1-Dimethylethoxy)Carbonyl]amino]-, (2E,4s)-(9CI)
  • N-Boc-L-alaninol
  • Boc-L-β-homoalanine
  • (S)-N-BOC-(2-CHLOROPHENYL)GLYCINE
  • N-(tert-Butoxycarbonyl)-L-alanine
  • (R)-TERT-BUTYL 1-(ETHYLAMINO)PROPAN-2-YLCARBAMATE
  • (S)-tert-butyl 1-(methylamino)propan-2-ylcarbamate
  • tert-butyl 2,5-dimethylpyrrole-1-carboxylate

Articles

Synthesis of the C(26)-C(32) Oxazole Fragment of Calyculin C: A Test Case for Oxazole Syntheses.

J. Org. Chem. 63 , 92-98, (1998)

The synthesis of the C(26)-C(32) oxazole fragment 4 and its C(32) epimer 20 of serine/threonine protein phosphatase PP1 and PP2A inhibitor calyculin C is presented. The syn methyl arrangement in 4 was...

Synthesis of a C20-C26 segment of superstolide A by addition of a chiral allenylzinc reagent to (R)-N-boc alaninal.

Org. Lett. 7 , 1593-1596, (2005)

[reaction: see text] Additions of chiral allenylzinc and indium reagents to N-Boc alaninal were examined as a possible route to a C20-C26 segment of superstolide A. Allenylzinc reagents, prepared in s...

Practical syntheses of a CXCR3 antagonist.

J. Org. Chem. 76 , 1767-1774, (2011)

Two new, reliable syntheses of a pyrido[2,3-d]-pyrimidine inhibitor of the CXCR3 receptor are described. A nine-step synthesis of the CXCR3 inhibitor (1) from 2-aminonicotinic acid was demonstrated on...


More Articles


Related Compounds

  • BOC-L-ALANINAL
  • Boc-L-aspartic acid 4-benzyl ester
  • Boc-L-Thr(Bzl)-D-Leu-OMe
  • Boc-L-Tyrosine methyl ester
  • Boc-L-Glutamine
  • Boc-L-Asp(Bzl)-ONp
  • 2-{[(2-Iodocycloheptyl)oxy]methyl}oxolane
  • tert-butyl N-{3-iodo-2-methyl-2-[(oxolan-2-yl)methoxy]propyl}carbamate
  • 3-Iodo-4-[(oxolan-2-yl)methoxy]-1lambda6-thiolane-1,1-dione
  • 3-Bromo-4-[(oxolan-2-yl)methoxy]oxolane
  • 3-Iodo-4-[(oxolan-2-yl)methoxy]oxolane
  • 2-{[(3-Bromo-1,4-dichlorobutan-2-yl)oxy]methyl}oxolane
  • Tert-butyl 3-bromo-4-[2-(propan-2-yloxy)ethoxy]pyrrolidine-1-carboxylate
  • 1-Iodo-2-[2-(propan-2-yloxy)ethoxy]cyclopentane
  • tert-butyl N-{3-bromo-2-methyl-2-[2-(propan-2-yloxy)ethoxy]propyl}carbamate
  • 4-(Bromomethyl)-4-[2-(propan-2-yloxy)ethoxy]oxane
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.