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00848

(1R,4S)-cis-4-Acetoxy-2-cyclopenten-1-ol

≥98.0% (sum of enantiomers, GC)

Synonym(s):

(1S,4R)-cis-4-Hydroxy-2-cyclopentenyl acetate

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Size/SKUAvailabilityPrice
500 mg
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$793.00

About This Item

Empirical Formula (Hill Notation):
C7H10O3
CAS Number:
Molecular Weight:
142.15
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4350633

$793.00


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Quality Segment

assay

≥98.0% (sum of enantiomers, GC)

optical activity

[α]20/D −67±2°, c = 2.3% in chloroform

mp

49-51 °C

functional group

ester, hydroxyl

SMILES string

CC(=O)O[C@H]1C[C@@H](O)C=C1

InChI

1S/C7H10O3/c1-5(8)10-7-3-2-6(9)4-7/h2-3,6-7,9H,4H2,1H3/t6-,7+/m0/s1

InChI key

IJDYOKVVRXZCFD-NKWVEPMBSA-N

Application

(1R,4S)-cis-4-Acetoxy-2-cyclopenten-1-ol can be used as a reactant in the total synthesis of Bartlett′s brefeldin intermediate, spinosyn A analogs, (+)-7-deaza-5′-noraristeromycin, (±) strychnine and the Wieland-Gumlich aldehyde.

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This Item
44604129823PHR2421
description

≥98.0% (sum of enantiomers, GC)

description

≥99%

description

≥99.0% (GC)

description

-

functional group

hydroxyl, ester

functional group

-

functional group

hydroxyl

functional group

-

optical activity

[α]20/D −67±2°, c = 2.3% in chloroform

optical activity

[α]20/D +68°, c = 2.3 in chloroform

optical activity

-

optical activity

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

300

mp

49-51 °C

mp

49-51 °C (lit.)

mp

55-59 °C

mp

-

assay

≥98.0% (sum of enantiomers, GC)

assay

≥99%

assay

≥99.0% (GC)

assay

-


Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

Eyeshields, Gloves, type N95 (US)

flash_point_f

No data available

flash_point_c

No data available



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