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methyl (2S)-3-azido-2-methylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107747-84-2 Structure
  • Basic information

    1. Product Name: methyl (2S)-3-azido-2-methylpropanoate
    2. Synonyms: Methyl (2S)-3-azido-2-methylpropanoate; propanoic acid, 3-azido-2-methyl-, methyl ester, (2S)-
    3. CAS NO:107747-84-2
    4. Molecular Formula: C5H9N3O2
    5. Molecular Weight: 143.1439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107747-84-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl (2S)-3-azido-2-methylpropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2S)-3-azido-2-methylpropanoate(107747-84-2)
    11. EPA Substance Registry System: methyl (2S)-3-azido-2-methylpropanoate(107747-84-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 107747-84-2(Hazardous Substances Data)

107747-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107747-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,4 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 107747-84:
(8*1)+(7*0)+(6*7)+(5*7)+(4*4)+(3*7)+(2*8)+(1*4)=142
142 % 10 = 2
So 107747-84-2 is a valid CAS Registry Number.

107747-84-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-3-azido-2-methylpropionic acid methyl ester

1.2 Other means of identification

Product number -
Other names (S)-methyl 3-azido-2-methylpropanoate

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:107747-84-2 SDS

107747-84-2Downstream Products

107747-84-2Relevant articles and documents

Two Biosynthetic Pathways in Jahnella thaxteri for Thaxteramides, Distinct Types of Lipopeptides

Oueis, Emilia,Klefisch, Thorsten,Zaburannyi, Nestor,Garcia, Ronald,Plaza, Alberto,Müller, Rolf

, p. 5407 - 5412 (2019)

The structures of five linear lipopeptides, thaxteramides A1, A2, B1, B2, and C isolated from the myxobacterium Jahnella thaxteri, were elucidated. They have a C-terminal common tetrapeptidic Tyr-Gly-β-Ala-Tyr core but differ in the stereochemistry of the

Oligomers of N-Substituted β2-Homoalanines: Peptoids with Backbone Chirality

Lee, Kang Ju,Lee, Woo Sirl,Yun, Hyosuk,Hyun, Yu-Jung,Seo, Chang Deok,Lee, Chul Won,Lim, Hyun-Suk

, p. 3678 - 3681 (2016)

A new class of peptoid-based peptidomimetics composed of oligomers of N-substituted β2-homoalanines is reported. Design, solid-phase synthesis, and preliminary circular dichroism studies of oligomers of N-alkylated β2-homoalanines co

Synthesis of sterically hindered amine containing azide via chemoselective hydride reduction

Kim, Hwa-Ok

, p. 1713 - 1720 (1998)

The chemoselective reduction of an ester in the presence of an azido group by LiCl/NaBH4 is described. A sterically hindered secondary amine containing an azido group is synthesized by this method.

Structural modification of the P2′ position of 2,7-dialkyl- substituted 5(S)-amino-4(S)-hydroxy-8-phenyl-octanecarboxamides: The discovery of aliskiren, a potent nonpeptide human renin inhibitor active after once daily dosing in marmosets

Maibaum, Jürgen,Stutz, Stefan,G?schke, Richard,Rigollier, Pascal,Yamaguchi, Yasuchika,Cumin, Frédéric,Rahuel, Joseph,Baum, Hans-Peter,Cohen, Nissim-Claude,Schnell, Christian R.,Fuhrer, Walter,Gruetter, Markus G.,Schilling, Walter,Wood, Jeanette M.

, p. 4832 - 4844 (2008/03/12)

Due to its function in the rate limiting initial step of the renin-angiotensin system, renin is a particularly promising target for drugs designed to control hypertension, a growing risk to health worldwide. Despite vast efforts over more than two decades

DIPEPTIDYL PEPTIDASE-IV INHIBITING COMPOUNDS, METHODS OF PREPARING THE SAME, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME AS AN ACTIVE AGENT

-

Page/Page column 28-29, (2010/11/24)

The present invention relates to novel compounds exhibiting good inhibitory activity versus Dipeptidyl Peptidase-IV(DPP-IV), methods of preparing the same and pharmaceutical compositions containing the same as an active agent.

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