ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >Serine derivatives >L-Ser-OBzl.HCl

L-Ser-OBzl.HCl

L-Ser-OBzl.HCl Structure
CAS No.
60022-62-0
Chemical Name:
L-Ser-OBzl.HCl
Synonyms
H-SER-OBZL·HCL;H-SER-OBZL HCL;SERINE-OBZL HCL;H-L-Ser-OBzl.HCl;L-SerinebenzylesterHCl;H-L-Ser-Obzl*Hydrochloride;L-SERINE BENZYL ESTER HYDROCHLORIDE;L-SerineBenzylEsterHydrochloride>Benzyl serinate hydrochloride (1:1);benzyl (2S)-2-amino-3-hydroxypropanoate
CBNumber:
CB2286886
Molecular Formula:
C10H14ClNO3
Molecular Weight:
231.68
MOL File:
60022-62-0.mol
Modify Date:
2024/4/23 19:22:53

L-Ser-OBzl.HCl Properties

Melting point 175°C
refractive index -12 ° (C=1, H2O)
storage temp. Inert atmosphere,Store in freezer, under -20°C
form powder to crystal
color White to Almost white
Water Solubility Soluble in water.
InChI InChI=1/C10H13NO3.ClH/c11-9(6-12)10(13)14-7-8-4-2-1-3-5-8;/h1-5,9,12H,6-7,11H2;1H/t9-;/s3
InChIKey MGZWCDQAKCHOBX-FVGYRXGTSA-N
SMILES C(OCC1=CC=CC=C1)(=O)[C@H](CO)N.[H]Cl |&1:10,r|
CAS DataBase Reference 60022-62-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Safety Statements  24/25
WGK Germany  3
HS Code  29225090
NFPA 704
1
0 0

L-Ser-OBzl.HCl price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S5633 L-Serine benzyl ester hydrochloride 60022-62-0 5G ₹10576.03 2022-06-14 Buy
Sigma-Aldrich(India) S5633 L-Serine benzyl ester hydrochloride 60022-62-0 25G ₹35982.3 2022-06-14 Buy
TCI Chemicals (India) S0550 L-Serine Benzyl Ester Hydrochloride 60022-62-0 5G ₹6000 2022-05-26 Buy
Product number Packaging Price Buy
S5633 5G ₹10576.03 Buy
S5633 25G ₹35982.3 Buy
S0550 5G ₹6000 Buy

L-Ser-OBzl.HCl Chemical Properties,Uses,Production

Description

L-Serine benzyl ester hydrochloride, also known as L-Serine-Bz-HCl, is a derivative of the amino acid L-Serine. It is a water-soluble, white crystalline powder and is commonly used as a reagent in biochemical and physiological studies. It is a useful raw material that could synthesize mang organic compounds, such as a cyclic sulfamidate which could reacted cleanly with the sodium thiolate salt of a variety of unprotected 1-thio sugars in aqueous buffer to afford the corresponding S-linked amino acid glycoconjugates in good yields after hydrolysis of the N-sulfates[1].
L-Serine benzyl ester hydrochloride

Chemical Properties

Colorless solid

Uses

It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff.

Preparation

Boc-L-Ser-OBz (2.953 g, 10 mmol) was dissolved in MeOH (21 mL) and was palced in ice bath. Then concentrated hydrochloric acid (4.25 mL) was added dropwise. The ice bath was removed and the reaction mixture was stirred for 3 hours. After that the isopropanol (10 mL) was added and the volatile components were removed under reduced pressure at 55 ℃. The oily residue was coevaporated with isopropanol three times (3x10 mL). L-Serine benzyl ester hydrochloride ( yield=69%) was crystallized from H2O/iPr-OH/acetone mixture.
L-Serine benzyl ester hydrochloride

References

[1] Cohen S, et al. Synthesis of S-linked glycosyl amino acids in aqueous solution with unprotected carbohydrates. Organic Letters, 2001; 3: 405–407.

L-Ser-OBzl.HCl Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 184)Suppliers
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ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32835 60 Inquiry
SERINE-OBZL HCL L-SERINE BENZYL ESTER HYDROCHLORIDE H-SER-OBZL HCL benzyl 2-aMino-3-hydroxypropanoate hydrochloride H-SER-OBZL·HCL L-SerinebenzylesterHCl L-Serine benzyl ester hydrochloride≥ 99% (TLC) L-β-Hydroxyalanine benzyl ester hydrochloride benzyl (2S)-2-amino-3-hydroxypropanoate hydrochloride L-SerineBenzylEsterHydrochloride> benzyl (2S)-2-amino-3-hydroxypropanoate H-L-Ser-Obzl*Hydrochloride (S)-2-amino-3-hydroxypropionyloxybenzylhydrochloride Benzyl serinate hydrochloride (1:1) H-L-Ser-OBzl.HCl L-Serine Benzyl Ester Hydrochloride,95% 60022-62-0 Amino Acid Benzyl Esters Amino Acids Amino Acids (C-Protected) Biochemistry