57092-20-3

Post Buying Request

Basic information

Product Name: BOC-LEU-MET-OH
Synonyms: BOC-LEU-MET-OH;Boc-L-Met-L-Leu-OH
CAS NO:57092-20-3
Molecular Formula: C16H30N2O5S
Molecular Weight: 362.48
EINECS: N/A
Product Categories: N/A
Mol File: 57092-20-3.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: 576.1±50.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: 1.130±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: 3.33±0.10(Predicted)
CAS DataBase Reference: BOC-LEU-MET-OH(CAS DataBase Reference)
NIST Chemistry Reference: BOC-LEU-MET-OH(57092-20-3)
EPA Substance Registry System: BOC-LEU-MET-OH(57092-20-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 57092-20-3(Hazardous Substances Data)

Suppliers
Usage
SDS
Upstream product
Downstream Products
Article

57092-20-3 Suppliers

Recommended suppliersmore

Product
FOB Price
Min.Order
Supply Ability
Supplier
Contact Supplier

Boc-Met-Leu-oh cas no.57092-20-3 0.98
Cas No: 57092-20-3
No Data
No Data
No Data
Win-Win chemical Co.Ltd
Contact Supplier

(2s)-2-[[(2s)-4-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoyl]amino]-4-methylsulfanylbutanoic Acid
Cas No: 57092-20-3
No Data
No Data
No Data
Suzhou Health Chemicals Co., Ltd.
Contact Supplier

(2S)-2-[[(2S)-4-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoyl]amino]-4-methylsulfanylbutanoic acid
Cas No: 57092-20-3
No Data
No Data
No Data
Research Peptide Biotechnology Co., Ltd.
Contact Supplier

BOC-LEU-MET-OH
Cas No: 57092-20-3
No Data
No Data
No Data
ZHEJIANG JIUZHOU CHEM CO.,LTD
Contact Supplier

BOC-LEU-MET-OH
Cas No: 57092-20-3
No Data
10 Gram
1 Metric Ton/Month
Sichuan Jiayinglai Technology Co,Ltd (Enlai Biotech)
Contact Supplier

57092-20-3 Usage

Description

BOC-LEU-MET-OH, also known as N-tert-butoxycarbonyl-L-leucyl-L-methionine methyl ester, is a peptide derivative that serves as a protected form of the amino acids leucine and methionine for peptide synthesis. The t-butoxycarbonyl (BOC) group acts as a protecting group for the amine and carboxylic acid of the amino acids, preventing unwanted reactions during peptide synthesis. This chemical is an important tool in the construction of peptides and proteins in laboratory settings for various research and industrial applications.
Used in Biochemistry and Molecular Biology:
BOC-LEU-MET-OH is used as a protected amino acid derivative for peptide synthesis, allowing for the controlled and efficient assembly of peptide sequences in laboratory settings.
Used in Pharmaceutical Industry:
BOC-LEU-MET-OH is used as a building block for the development of peptide-based drugs, facilitating the synthesis of therapeutic agents with specific biological activities.
Used in Research and Development:
BOC-LEU-MET-OH is used as a research tool for studying the structure, function, and interactions of peptides and proteins, contributing to a better understanding of biological processes and the development of new therapeutic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 57092-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57092-20:
(7*5)+(6*7)+(5*0)+(4*9)+(3*2)+(2*2)+(1*0)=123
123 % 10 = 3
So 57092-20-3 is a valid CAS Registry Number.

57092-20-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	(2S)-2-[[(2S)-4-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoyl]amino]-4-methylsulfanylbutanoic acid

1.2 Other means of identification

Product number	-
Other names	Boc-Leu-Met-OH

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57092-20-3 SDS

57092-20-3Upstream product

2280-69-5 Boc-Leu-Met-OMe

57092-20-3Downstream Products

57092-20-3Relevant articles and documents

Synthesis of cyclic and cyclically branched tachykinine partial sequences. Part I: Synthesis of the homodet-cyclic eledoisin(6-11)-hexapeptide

Neubert,Bergmann,Mansfeld,Hartrodt,Barth,Jakubke

, p. 456 - 459 (2007/10/02)

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 57092-20-3