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

Click to get detail 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

Click to get detail 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
  • 2-Amino-3-(3-chloro-5-fluorophenyl)-2-methylpropan-1-ol
  • O-{[1-(dimethyl-1,3-oxazol-2-yl)cyclopropyl]methyl}hydroxylamine
  • 1-{4-[4-(difluoromethyl)-1-ethyl-1H-pyrazol-3-yl]phenyl}ethan-1-amine
  • 1-[1-(1-Methylcyclopropyl)ethyl]cyclopropan-1-amine
  • O-[2-(1H-imidazol-2-yl)-2-methylpropyl]hydroxylamine
  • N-[2-(3-aminocyclopentyl)ethyl]-2-nitrobenzene-1-sulfonamide
  • 5-(3,4-Dichlorophenyl)-2-pyridinecarboxamide
  • N-(3-aminobutan-2-yl)-2-nitrobenzene-1-sulfonamide
  • Tert-butyl 2-[(6-{[5-chloro-2-(piperazin-1-yl)pyrimidin-4-yl]amino}-1-methyl-2-oxo-1,2-dihydroquinolin-3-yl)oxy]acetate
  • 2-[2-Methoxy-5-(trifluoromethyl)phenyl]acetaldehyde