(S)-N-ALPHA-T-BUTYLOXYCARBONYL-3-BROMO-PHENYLALANINE

(S)-N-ALPHA-T-BUTYLOXYCARBONYL-3-BROMO-PHENYLALANINE - Names and Identifiers

Name	(S)-N-BOC-3-Bromophenylalanine
Synonyms	BOC-PHE(3-BR)-OH BOC-L-3-BROMOPHE BOC-S-PHE(3-BR)-OH Boc-L-3-Bromophenylalanine BOC-L-3-BROMOPHENYLALANINE BOC-3-BROMO-L-PHENYLALANINE Boc-3-Bromo-L-phenylalanine (S)-N-BOC-3-BROMOPHENYLALANINE (S)-N-BOC-3-Bromophenylalanine (S)-N-ALPHA-T-BUTYLOXYCARBONYL-3-BROMO-PHENYLALANINE (S)-3-(3-BROMO-PHENYL)-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID
CAS	82278-73-7
EINECS	1592732-453-0
InChI	InChI=1/C14H18BrNO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-5-4-6-10(15)7-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/p-1/t11-/m0/s1

(S)-N-ALPHA-T-BUTYLOXYCARBONYL-3-BROMO-PHENYLALANINE - Physico-chemical Properties

Molecular Formula	C14H18BrNO4
Molar Mass	344.2
Density	1.5311 (rough estimate)
Melting Point	106.1°C
Boling Point	475.3±40.0 °C(Predicted)
Flash Point	241.2°C
Water Solubility	Slightly soluble in water.
Vapor Presure	7.71E-10mmHg at 25°C
pKa	3.81±0.10(Predicted)
Storage Condition	Sealed in dry,Room Temperature
Refractive Index	1.6500 (estimate)

(S)-N-ALPHA-T-BUTYLOXYCARBONYL-3-BROMO-PHENYLALANINE - Risk and Safety

Safety Description	S24/25 - Avoid contact with skin and eyes.
Hazard Class	IRRITANT

(S)-N-ALPHA-T-BUTYLOXYCARBONYL-3-BROMO-PHENYLALANINE - Introduction

(S)-N-BOC-3-Bromophenylalanine is an organic compound having the formula C11H13BrNO4.

Nature:
(S)-N-BOC-3-Bromophenylalanine is a white crystalline solid with good solubility. It has a melting point of about 140-142°C and has good thermal stability.

Use:
(S)-N-BOC-3-Bromophenylalanine is a common amino acid derivative, which has a wide range of applications in the field of organic synthesis. It is often used as a chiral intermediate or starting material for the preparation of chiral drugs, peptides and bioactive molecules.

Preparation Method:
The preparation of (S)-N-BOC-3-Bromophenylalanine is usually achieved by chemical synthesis. A common method is to first react L-phenylalanine with imatine bromide to obtain L-3-bromophenylalanine, and then add a Boc protecting group to react to generate the target product (S)-N-BOC-3-Bromophenylalanine.

Safety Information:
Since (S)-N-BOC-3-Bromophenylalanine is a chemical, it should be handled with caution. When using, it is necessary to comply with relevant laboratory safety regulations and operating guidelines. In addition, avoid contact with skin and eyes, and ensure that you operate in a well-ventilated environment. If ingestion or mistake into the eye, should seek medical attention immediately.

Last Update：2024-04-09 21:04:16