Welcome to LookChem.com Sign In|Join Free

CAS

  • or

263870-93-5

Post Buying Request

263870-93-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

263870-93-5 Usage

Description

(S)-2-Amino-4-penten-1-ol, also known as L-2-amino-4-penten-1-ol or 2-amino-4-penten-1-ol, is a colorless liquid chemical compound with the molecular formula C5H11NO. It is characterized by an amine odor and is recognized as a chiral, non-proteinogenic amino alcohol. (S)-2-Amino-4-penten-1-ol is highly valued in the field of organic chemistry and chemical synthesis due to its stereochemistry, which enables its use in asymmetric synthesis, and its role as an important intermediate in the creation of various complex organic molecules.

Uses

Used in Pharmaceutical Synthesis:
(S)-2-Amino-4-penten-1-ol is used as a chiral building block for the synthesis of pharmaceuticals. Its unique stereochemistry allows for the creation of complex organic molecules that are essential in the development of new drugs and medications.
Used in Agrochemical Production:
(S)-2-Amino-4-penten-1-ol is also utilized in the production of agrochemicals, which are chemicals specifically designed to benefit crop or livestock production, such as pesticides, fertilizers, and other agricultural aids.
Used in Fragrance and Flavor Industries:
(S)-2-Amino-4-penten-1-ol is employed in the creation of fragrances and flavors, where its unique properties contribute to the development of novel and distinct scents and tastes for various consumer products.
Used in Asymmetric Synthesis:
Due to its stereochemistry, (S)-2-Amino-4-penten-1-ol is a valuable intermediate in asymmetric synthesis, a technique that allows for the selective production of one enantiomer of a molecule over another. This selective synthesis is crucial in the development of enantiomerically pure compounds, which can have different biological activities and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 263870-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,8,7 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 263870-93:
(8*2)+(7*6)+(6*3)+(5*8)+(4*7)+(3*0)+(2*9)+(1*3)=165
165 % 10 = 5
So 263870-93-5 is a valid CAS Registry Number.

263870-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-allylglycinol

1.2 Other means of identification

Product number -
Other names (S)-2-Amino-pent-4-en-1-ol

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:263870-93-5 SDS

263870-93-5Relevant articles and documents

FUSED TRICYCLIC HETEROCYCLE COMPOUNDS AND THERAPEUTIC USES THEREOF

-

Page/Page column 56; 102-103, (2020/01/24)

This application discloses a new class of fused tricyclic heterocycles of formula (I), preparation methods thereof, pharmaceutical compositions comprising these compounds, and pharmaceutically acceptable salts, solvates, or prodrugs thereof, and their use

Two phenyls are better than one or three: Synthesis and application of terminal olefin-oxazoline (TOlefOx) ligands

Zhao, Yi-Shuang,Liu, Jian-Kang,He, Zhi-Tao,Tao, Jing-Chao,Tian, Ping,Lin, Guo-Qiang

supporting information, p. 3686 - 3689 (2016/05/09)

A novel terminal olefin-oxazoline ligand was introduced into rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to enones and gave excellent enantioselectivities. The two phenyls proved better than one or three in ligand evaluations.

AZABICYCLO [4.1.0] HEPT - 4 - YL DERIVATIVES AS HUMAN OREXIN RECEPTOR ANTAGONISTS

-

Page/Page column 27, (2012/07/14)

This invention relates to azabicyclo[4.1.0]hept-4-yl derivatives and their use as pharmaceuticals.

Post a RFQ

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)

1

What can I do for you?
Get Best Price

Get Best Price for 263870-93-5