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Benzyl N-(2-hydroxyethyl)carbamate

CAS No.
77987-49-6
Chemical Name:
Benzyl N-(2-hydroxyethyl)carbamate
Synonyms
Benzyl (2-hydroxyethyl)carbaMate;2-(CARBOBENZOXYAMINO)-1-ETHANOL;Z-GLY-OL;Z-GLYCINOL;N-Z-ETHANOLAMINE;Cbz-Gly-OL;Z-NH-(CH2)2-OH;Z-ETHANOLAMINE;Z-AMINOETHANOL;N-CBZ-GLYCINOL
CBNumber:
CB6201850
Molecular Formula:
C10H13NO3
Molecular Weight:
195.22
MDL Number:
MFCD00191060
MOL File:
77987-49-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:54:01

Benzyl N-(2-hydroxyethyl)carbamate Properties

Melting point 58-60 °C (lit.)
Boiling point 215 °C/15 mmHg (lit.)
Density 1.1926 (rough estimate)
refractive index 1.5150 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Soluble in water or 1% acetic acid
pka 11.80±0.46(Predicted)
form Powder
color White
BRN 2050891
InChI InChI=1S/C10H13NO3/c12-7-6-11-10(13)14-8-9-4-2-1-3-5-9/h1-5,12H,6-8H2,(H,11,13)
InChIKey SAGINAGERRNGGV-UHFFFAOYSA-N
SMILES C(OCC1=CC=CC=C1)(=O)NCCO
CAS DataBase Reference 77987-49-6(CAS DataBase Reference)
UNSPSC Code 12352200

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
HS Code  29221985
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
0
2 0

Benzyl N-(2-hydroxyethyl)carbamate price More Price(60)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 407909 N-Z-Ethanolamine 98% 77987-49-6 5g $35 2023-06-20 Buy
Sigma-Aldrich 407909 N-Z-Ethanolamine 98% 77987-49-6 25g $40 2023-06-20 Buy
TCI Chemical H0793 2-(Carbobenzoxyamino)-1-ethanol >97.0%(GC) 77987-49-6 5g $62 2026-04-30 Buy
TCI Chemical H0793 2-(Carbobenzoxyamino)-1-ethanol >97.0%(GC) 77987-49-6 25g $244 2026-04-30 Buy
Usbiological 457370 N-(Benzyloxycarbonyl)ethanolamine 77987-49-6 1g $312 2026-06-03 Buy
Product number Packaging Price Buy
407909 5g $35 Buy
407909 25g $40 Buy
H0793 5g $62 Buy
H0793 25g $244 Buy
457370 1g $312 Buy

Benzyl N-(2-hydroxyethyl)carbamate Chemical Properties,Uses,Production

Chemical Properties

White powder

Uses

N-(Benzyloxycarbonyl)ethanolamine is an intermediate used to prepare alkynylaryladenines as A2A adenosine receptor agonists and effects on hepatic glucose production. It is also used in the synthesis of functionalized N-arylaminoethyl amides as noncovalent inhibitors of cathepsin S.

reaction suitability

reagent type: cross-linking reagent

Synthesis

Monoethanolamine

141-43-5

Benzyl chloroformate

501-53-1

BENZYL N-(2-HYDROXYETHYL)CARBAMATE

77987-49-6

(1) Synthesis of benzyl [2-(tert-butyldiphenylmethoxysilyl)ethyl]carbamate [1515]: To a solution of 2-aminoethanol (2.0 g, 32.7 mmol) in dichloromethane (60 mL), benzyl chloroformate (5.6 mL, 41.3 mmol) and triethylamine (5.5 mL, 39.5 mmol) were sequentially added under ice bath conditions. The reaction mixture was stirred at room temperature for 1 hour. After completion of the reaction, the mixture was partitioned between ethyl acetate and saturated aqueous sodium chloride solution. The organic layer was dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with the eluent being toluene:acetonitrile (3:2) to afford benzyl (2-hydroxyethyl)carbamate (5.37 g, 84% yield) as a white solid. [1516] Subsequently, to a solution of benzyl (2-hydroxyethyl)carbamate (5.37 g, 27.5 mmol) in dimethylformamide (160 mL) was added tert-butyldiphenylmethylsilyl chloride (8.6 mL, 33.0 mmol) and imidazole (2.3 g, 33.8 mmol) under ice bath conditions. The mixture was stirred at room temperature overnight. After the reaction was complete, ethanol was added and stirring was continued for 2 hours. The reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with hexane:ethyl acetate (5:1) as eluent to give benzyl [2-(tert-butyldiphenylmethylsilylmethoxy)ethyl]carbamate (11.93 g, 100% yield) as a colorless transparent syrup. [1517] 1H-NMR (400 MHz, CDCl3): δ (ppm) 7.64 (4H, d, J = 6.8 Hz), 7.46-7.28 (12H, m), 5.10 (2H, s), 3.73 (2H, t, J = 4.9 Hz), 3.35 (2H, q, J = 4.9 Hz), 1.05 (9H, s).

References

[1] Patent: US2004/14962, 2004, A1. Location in patent: Page/Page column 137
[2] Journal of Organic Chemistry, 1987, vol. 52, # 7, p. 1252 - 1255
[3] Bioorganic and Medicinal Chemistry Letters, 2000, vol. 10, # 15, p. 1749 - 1750
[4] Tetrahedron Letters, 2007, vol. 48, # 46, p. 8170 - 8173
[5] Tetrahedron, 1991, vol. 47, # 14/15, p. 2591 - 2602

Benzyl N-(2-hydroxyethyl)carbamate Preparation Products And Raw materials

Global( 185)Suppliers
Supplier Tel Email Country ProdList Advantage
Hangzhou Cheminspire Technology Co., Ltd. 0571-89081561; 10006559855 info@cheminspire.com China 412 58
Taizhou Wealsun Biotech Co., Ltd 18351140886; 18351140886 wealsunbio@126.com China 139 58
Chengdu jingzhihuacheng Chemical Technology Co., Ltd. 028-37664989 15900794981 873239557@qq.com China 1050 58
Shanghai Hobor Chemical Co., Ltd 13918007836 sales@hoborchem.com China 423 60
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Ark Pharm, Inc. 847-367-3680 sales@arkpharminc.com United States 1669 56
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
GL Biochem (Shanghai) Ltd 21-61263452 13641803416 ymbetter@glbiochem.com China 9981 64

View Lastest Price from Benzyl N-(2-hydroxyethyl)carbamate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cbz-Gly-ol pictures 2026-09-11 Cbz-Gly-ol
77987-49-6
1kg 98% 1T+ Sichuan HongRi Pharma-Tech Co.,Ltd
BENZYL N-(2-HYDROXYETHYL)CARBAMATE pictures 2025-04-04 BENZYL N-(2-HYDROXYETHYL)CARBAMATE
77987-49-6
1KG 98% 1ton Henan Aochuang Chemical Co.,Ltd.
Z-Gly-ol pictures 2020-01-06 Z-Gly-ol
77987-49-6
$1.00 1g 98% 100KG Sichuan Jiaying Lai Technology Co.,LTD
  • Cbz-Gly-ol pictures
  • Cbz-Gly-ol
    77987-49-6
  • 98%
  • Sichuan HongRi Pharma-Tech Co.,Ltd
  • Z-Gly-ol pictures
  • Z-Gly-ol
    77987-49-6
  • $1.00
  • 98%
  • Sichuan Jiaying Lai Technology Co.,LTD
Z-AMINOETHANOL Z-ETHANOLAMINE Z-GLY-OL Z-GLYCINOL Z-NH-(CH2)2-OH 2-(CBZ-AMINO)-1-ETHANOL 2-(CARBOBENZOXYAMINO)-1-ETHANOL 2-(Z-AMINO)-ETHANOL N-CARBOBENZOXY-2-AMINOETHANOL N-CARBOBENZOXY-GLYCINOL N-(2-HYDROXYETHYL)CARBAMIC ACID BENZYL ESTER LABOTEST-BB LT00452296 N-CBZ-GLYCINOL 2-(Z-Amino)ethanol, Benzyl N-(2-hydroxyethyl)carbamate 2-(Benzyloxycarbonylamino)-1-ethanol Benzyl N-(2-Hydroxyethyl)carbamate 2-(Cbz-amino)-1-ethanol N-(2-Hydroxyethyl)carbamic Acid Benzyl Ester N-(2-hydroxyethyl)carbamic acid (phenylmethyl) ester N-Z-EthanolaMine 98% Cbz-Gly-OL (2-Hydroxy-ethyl)-carbamic acid benzyl ester Z-Glycinol≥ 99% (HPLC) 2-(Cbz-amino)ethanol N - (benzyloxycarbonylamino) - 1-ethanol 2-(Carbobenzoxyamino)-1-ethanol> Carbamic acid, N-(2-hydroxyethyl)-, phenylmethyl ester BENZYL N-(2-HYDROXYETHYL)CARBAMATE USP/EP/BP N-Z-Ethanolamine Benzyl (2-hydroxyethyl)carbaMate N-Z-ETHANOLAMINE Benzyl N-(2-hydroxyethyl)carbamate 77987-49-6 HOCH2CH2NHCO2CH2C6H5 Oxygen Compounds Organic Building Blocks Building Blocks Amino Alcohols Z-Amino acid series Amino Alcohols Bifunctional Crosslinkers Building Blocks Chemical Biology Chemical Synthesis Linkers Organic Building Blocks Oxygen Compounds Peptide Chemistry Cbz-PEG