H-Ser-Ome·HCl

Modify Date: 2024-01-04 18:05:19

H-Ser-Ome·HCl Structure
H-Ser-Ome·HCl structure
Common Name H-Ser-Ome·HCl
CAS Number 5680-80-8 Molecular Weight 155.580
Density N/A Boiling Point 234.7ºC at 760 mmHg
Molecular Formula C4H10ClNO3 Melting Point 160-165ºC
MSDS Chinese USA Flash Point 95.8ºC

 Use of H-Ser-Ome·HCl


L-Serine methyl ester (hydrochloride) is a serine derivative[1].

 Names

Name L-Serine methyl ester hydrochloride
Synonym More Synonyms

 H-Ser-Ome·HCl Biological Activity

Description L-Serine methyl ester (hydrochloride) is a serine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

 Chemical & Physical Properties

Boiling Point 234.7ºC at 760 mmHg
Melting Point 160-165ºC
Molecular Formula C4H10ClNO3
Molecular Weight 155.580
Flash Point 95.8ºC
Exact Mass 155.034927
PSA 72.55000
Storage condition -20°C

 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 S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 29225000

 Synthetic Route

~98%

H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: Tetrahedron, , vol. 50, # 31 p. 9411 - 9424

~87%

H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: Journal of Organic Chemistry, , vol. 55, # 8 p. 2271 - 2272

~99%

H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: Chemical Communications, , vol. 46, # 3 p. 445 - 447

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H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: Tetrahedron Letters, , vol. 54, # 48 p. 6511 - 6513

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H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: US5113009 A1, ;

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H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: US5523463 A1, ;

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H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: Tetrahedron Letters, , vol. 29, # 2 p. 235 - 238

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H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: Synthesis, , # 19 art. no. P06210SS, p. 3353 - 3357

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H-Ser-Ome·HCl Structure

H-Ser-Ome·HCl

CAS#:5680-80-8

Literature: Synthesis, , # 19 art. no. P06210SS, p. 3353 - 3357

 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%

 Articles7

More Articles
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

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...

 Synonyms

L-Serine, methyl ester, hydrochloride (1:1)
MFCD00063680
methyl (2S)-2-amino-3-hydroxypropanoate,hydrochloride
DL-Serine, methyl ester, hydrochloride
Methyl L-serinate hydrochloride (1:1)
methyl DL-serinate hydrochloride
EINECS 227-140-7
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
H-Ser-OMe·HCl
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