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4-Penten-1-ol

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Catalog Number

ACM821090-2

Product Name

4-Penten-1-ol

Structure

CAS

821-09-0

Product Overview
Usage

Synonyms

S14-0957; UNII-W0558TQC6F; ACN-S003547; 4-Pentenol; TC-060303; InChI=1/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2; ZINC1632700; A840248; 821-09-0; CH2=CHCH2CH2CH₂OH;

IUPAC Name

pent-4-en-1-ol;

Molecular Weight

86.134g/mol

Molecular Formula

C5H10O;

Canonical SMILES

C=CCCCO;

InChI

InChI=1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2;

InChI Key

LQAVWYMTUMSFBE-UHFFFAOYSA-N;

Solubility

0.66 M;

Storage

2-8°C

Complexity

32.9

Covalently-Bonded Unit Count

EC Number

212-473-2

Exact Mass

86.073g/mol

H-Bond Acceptor

H-Bond Donor

Heavy Atom Count

Monoisotopic Mass

86.073g/mol

NSC Number

97503

Rotatable Bond Count

Topological Polar Surface Area

20.2A^2

UNII

W0558TQC6F

Application

4-Penten-1-ol is a colorless liquid that serves various roles in scientific and industrial applications. Primarily, it acts as a crucial reagent in carbohydrate chemistry, specifically in the n-Pentenyl Glycoside methodology, to facilitate the rapid assembly of homoglycans. This process is exemplified in forming the nonasaccharide component of high-mannose glycoproteins, playing a significant role in the synthesis of complex carbohydrates. Additionally, 4-Penten-1-ol is utilized in studying the epoxidation of olefins, with an oxo-diperoxo tungstate(VI) complex as a catalyst and bicarbonate as a co-catalyst. Its versatility extends to forming ester bonds at the C terminus of linear peptides in solutions using HATU as a coupling agent. Beyond its scientific applications, 4-Penten-1-ol finds usefulness in the agrochemical, pharmaceutical, and dyestuff industries, highlighting its multifunctional utility.

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CAS
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821-09-0
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