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192805

Sigma-Aldrich

1,3-Cyclopentanediol, mixture of cis and trans

95%

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About This Item

Linear Formula:
C5H8(OH)2
CAS Number:
Molecular Weight:
102.13
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

form

liquid

refractive index

n20/D 1.484 (lit.)

bp

80-85 °C/0.1 mmHg (lit.)

mp

40 °C (lit.)

density

1.094 g/mL at 25 °C (lit.)

SMILES string

OC1CCC(O)C1

InChI

1S/C5H10O2/c6-4-1-2-5(7)3-4/h4-7H,1-3H2

InChI key

NUUPJBRGQCEZSI-UHFFFAOYSA-N

Application

1,3-Cyclopentanediol was used in the synthesis of 1,3-cyclopentanediol bis(4-methylbenzenesulfonate) and β-hydroxy-substituted cyclic carbonyl compounds. It was also used in direct enantiomer resolution of diols without derivatization on a chiral polysiloxane by capillary gas chromatography.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Direct asymmetric a-hydroxylation of 2-hydroxymethyl ketones.
Paju A, et al.
Tetrahedron, 58(36), 7321-7326 (2002)
Direct resolution of enantiomeric diols by capillary gas chromatography on a chiral polysiloxane derived from (R, R)-tartramide.
Nakamura K, et al.
Analytical Chemistry, 62(5), 539-541 (1990)
Stepwise Introduction of p-Electron Cross-Conjugation: A Possible Access to [5] Radialenes?
Geneste F, et al.
The Journal of Organic Chemistry, 62(16), 5339-5343 (1997)

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