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CAS

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100017-22-9

(2R,3S)-1,2-Epoxy-3-hydroxy-4-pentene, also known as erythropentene, is a chiral organic compound characterized by the presence of an epoxy group and a hydroxyl group. Its specific (2R,3S) designation denotes the unique arrangement of atoms within the molecule, which is crucial for its reactivity and applications. Erythropentene's highly reactive nature, stemming from the epoxy group, allows it to participate in nucleophilic substitution reactions, making it a valuable chemical intermediate in the synthesis of pharmaceuticals and other organic compounds.

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  • 100017-22-9 Structure

  • Basic information

    1. Product Name: (2R,3S)-1,2-Epoxy-3-hydroxy-4-pentene
    2. Synonyms: (2R,3S)-1,2-Epoxy-3-hydroxy-4-pentene
    3. CAS NO:100017-22-9
    4. Molecular Formula:
    5. Molecular Weight: 100.117
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100017-22-9.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: (2R,3S)-1,2-Epoxy-3-hydroxy-4-pentene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3S)-1,2-Epoxy-3-hydroxy-4-pentene(100017-22-9)
    11. EPA Substance Registry System: (2R,3S)-1,2-Epoxy-3-hydroxy-4-pentene(100017-22-9)

  • 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: 100017-22-9(Hazardous Substances Data)

100017-22-9 Usage

Uses

Used in Pharmaceutical Synthesis:
Erythropentene is utilized as a chemical intermediate for the synthesis of various pharmaceuticals. Its reactivity and chiral properties enable the creation of complex molecules with specific biological activities, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, erythropentene serves as a versatile building block for constructing more elaborate organic compounds. Its ability to undergo nucleophilic substitution reactions allows chemists to incorporate it into the synthesis of a wide range of molecules, including those with potential applications in materials science, agrochemicals, and specialty chemicals.
Used in Chiral Chemistry:
The chiral nature of erythropentene makes it an important compound in chiral chemistry, where the spatial arrangement of atoms is critical for the compound's properties and reactivity. It can be used to study the effects of stereochemistry on reaction outcomes and to develop enantioselective synthetic methods for producing chiral molecules with specific biological activities or desired properties.

Check Digit Verification of cas no

The CAS Registry Mumber 100017-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,0,1 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 100017-22:
(8*1)+(7*0)+(6*0)+(5*0)+(4*1)+(3*7)+(2*2)+(1*2)=39
39 % 10 = 9
So 100017-22-9 is a valid CAS Registry Number.

100017-22-9SDS

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 (1S)-1-[(2R)-oxiran-2-yl]prop-2-en-1-ol

1.2 Other means of identification

Product number -
Other names (S)-1-((R)-Oxiran-2-yl)prop-2-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:100017-22-9 SDS

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