H-D-Ser-OMe.HCl

Suppliers

Names

[ CAS No. ]:
5874-57-7

[ Name ]:
H-D-Ser-OMe.HCl

[Synonym ]:
L-Serine, methyl ester, hydrochloride (1:1)
methyl (2S)-2-amino-3-hydroxypropanoate,hydrochloride
DL-Serine, methyl ester, hydrochloride
MFCD00066121
Methyl L-serinate hydrochloride (1:1)
methyl (2R)-2-amino-3-hydroxypropanoate,hydrochloride
methyl DL-serinate hydrochloride
Q1YZVO1 &&HCl
L-Serine, methyl ester, hydrochloride
Serine, methyl ester, hydrochloride (1:1)
Methyl serinate hydrochloride
Methyl serinate hydrochloride (1:1)
DL-serine methylester Hydrochloride
D-Serinemethylesterhydrochloride

Chemical & Physical Properties

[ Density]:
1.62g/cm3

[ Boiling Point ]:
234.7ºC at 760 mmHg

[ Melting Point ]:
163-166 °C(lit.)

[ Molecular Formula ]:
C4H10ClNO3

[ Molecular Weight ]:
155.580

[ Flash Point ]:
95.8ºC

[ Exact Mass ]:
155.034927

[ PSA ]:
72.55000

[ Index of Refraction ]:
1.693

MSDS

Safety Information

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

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29225000

Synthetic Route

Precursor & DownStream

Precursor

  • Methanol
  • D-serine
  • Acetyl chloride

DownStream

  • methyl (4R)-2-sulfanylidene-1,3-oxazolidine-4-carboxylate
  • Benzamide
  • BOC-D-SER-OME
  • Methyl N-[(benzyloxy)carbonyl]-D-serinate
  • methyl 2-amino-3-hydroxypropanoate

Customs

[ HS Code ]: 2922509090

[ Summary ]:
2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Acylated serine derivatives: a unique class of arthropod pheromones of the Australian redback spider, Latrodectus hasselti.

Angew. Chem. Int. Ed. Engl. 49(11) , 2037-40, (2010)

The novel and efficient direct synthesis of N,O-acetal compounds using a hypervalent iodine(III) reagent: an improved synthetic method for a key intermediate of discorhabdins.

Chem. Commun. (Camb.) (13) , 1764-6, (2005)

The use of hypervalent iodine(III) reagents allowed us to develop the novel and efficient direct synthesis of N,O-acetal compounds via the oxidative fragmentation reaction of alpha-amino acids or alph...

Aziridinium from N,N-dibenzyl serine methyl ester: synthesis of enantiomerically pure beta-amino and alpha,beta-diamino esters.

Org. Lett. 8(10) , 2183-6, (2006)

[reaction: see text] Reaction of N,N-dibenzyl-O-methylsulfonyl serine methyl ester with a variety of heteronucleophiles (sodium azide, sodium phthalimide, amines, thiols) and carbanions (sodium malona...


More Articles


Related Compounds

  • H-D-Ser-Obzl Hydrochloride salt
  • H-D-Ser(But)-Obut HCl
  • H-D-Ser(Bzl)-OH
  • H-D-Ser-OBzl.HCl
  • H-D-Ser(OBzl)-OH HCl
  • HD-Ser(tBu)-OMe * HCl
  • 3-Methylamino-thiophene-2-carboxylic acid amide
  • 1-(3-Methoxyphenyl)prop-2-yn-1-ol
  • (1S,2S,4S)-8,8-dimethylbicyclo[2.2.2]oct-5-en-2-ol
  • (2R)-2-(1,3-Benzodioxol-5-yl)propan-1-amine
  • 1-Acenaphthylenecarbonitrile, 2-methyl-
  • CID 11791012
  • 4-[(2-amino-1H-imidazol-1-yl)methyl]-Phenol
  • 4-Ethynylphenylacetone
  • N-[(1-Ethyl-1H-pyrazol-3-YL)methyl]-1-propyl-1H-pyrazol-3-amine
  • N-(1-cyanocyclohexyl)-N-methyl-2-(4H-1,2,4-triazol-3-ylsulfanyl)propanamide
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