N-(tert-butoxycarbonyl)-D-norleucine

N-(tert-butoxycarbonyl)-D-norleucine - Names and Identifiers

Name	boc-D-norleucine
Synonyms	Boc-D-Nle-OH boc-D-norleucine N-BOC-D-norleucine N-T-BOC-D-NORLEUCINE BOC-D-NORLEUCINE LIQUID N-BOC-(R)-2-AMINOHEXANOIC ACID N-(tert-butoxycarbonyl)-D-norleucine N-ALPHA-T-BUTOXYCARBONYL-D-NORLEUCINE N-alpha-tert-Butoxycarbonyl-D-norleucine N-ALPHA-TERT-BUTYLOXYCARBONYL-D-NORLEUCINE N-ALPHA-T-BUTOXYCARBONYL-D-2-AMINO-CAPROIC ACID N-ALPHA-T-BUTYLOXYCARBONYL-D-NORLEUCINE, (R)-N-ALPHA-BOC-2-AMINOHEXANOIC ACID
CAS	55674-63-0
InChI	InChI=1/C11H21NO4/c1-5-6-7-8(9(13)14)12-10(15)16-11(2,3)4/h8H,5-7H2,1-4H3,(H,12,15)(H,13,14)/t8-/m1/s1

N-(tert-butoxycarbonyl)-D-norleucine - Physico-chemical Properties

Molecular Formula	C11H21NO4
Molar Mass	231.29
Density	1.063±0.06 g/cm3(Predicted)
Boling Point	362.1±25.0 °C(Predicted)
Flash Point	172.8°C
Vapor Presure	3.14E-06mmHg at 25°C
pKa	4.02±0.21(Predicted)
Storage Condition	Sealed in dry,2-8°C
Refractive Index	1.462
Use	This product is for scientific research only and shall not be used for other purposes.

N-(tert-butoxycarbonyl)-D-norleucine - Risk and Safety

Safety Description	S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3
HS Code	29241990
Hazard Class	IRRITANT

N-(tert-butoxycarbonyl)-D-norleucine - Introduction

boc-D-norleucine (boc-D-norleucine) is an amino acid compound whose chemical structure contains an amino group and a carboxylic acid group. It is a derivative of D-norleucine, I .e. the carboxylic acid group on the D-norleucine is replaced by a temporary protecting group boc(tert-butyloxycarbonyl).

boc-D-norleucine is commonly used in biochemical research and peptide synthesis in organic synthesis. As an amino acid derivative, it can be used to construct a part of a polypeptide chain in order to study the structure and function of the polypeptide. In addition, it can also be used as an intermediate in the synthesis of drugs.

The general method for preparing boc-D-norleucine is to introduce a temporary protecting group boc on the carboxylic acid group of D-norleucine. The specific step is to D-norleucine and boc acid (tert-butyloxycarbamic acid) reaction, the use of amino acid amine reaction and acid reaction characteristics, the boc acid is introduced into the carboxylic acid group of D-norleucine.

Regarding safety information, boc-D-norleucine are laboratory chemicals and need to be operated under appropriate laboratory conditions. It is a colorless solid that may cause irritation to the eyes, skin and respiratory tract. When in use, it is recommended to wear appropriate protective equipment, such as goggles, gloves and laboratory coats. When stored, it should be kept in a dry, cool place, and away from fire and oxidizing agents. When handling and disposing of waste, relevant safe operating procedures should be observed.

Last Update：2024-04-09 20:02:46