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328316

Sigma-Aldrich

Cyclopentanecarbonyl chloride

98%

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Linear Formula:
C5H9COCl
CAS Number:
4524-93-0
Molecular Weight:
132.59
EC Number:
224-856-1
MDL number:
MFCD00001370
UNSPSC Code:
12352100
PubChem Substance ID:
24859728
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.4622 (lit.)

bp

161-162 °C (lit.)

density

1.091 g/mL at 25 °C (lit.)

SMILES string

ClC(=O)C1CCCC1

InChI

1S/C6H9ClO/c7-6(8)5-3-1-2-4-5/h5H,1-4H2

InChI key

WEPUZBYKXNKSDH-UHFFFAOYSA-N

Application

Cyclopentanecarbonyl chloride was used in preparation of:
  • 3′-N-acyl-7-trichloroacetyl-paclitaxels
  • cyclopentanecarboxylic acid 2-[5-(1-cyclopentane carbonyloxy-2-methyl-allyl)-2-oxo-dihydro-furan-3-yl-idene]-ethyl ester
  • cyclopentanecarboxylic acid 2-[5-(1-hydroxy-2-methyl allyl)-2-oxo-dihydro-furan-3-ylidene]-ethyl ester

Signal Word

Danger

Hazard Statements

H226,H314,H335

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

140.0 °F

Flash Point(C)

60 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

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Eun Joo Roh et al.
Bioorganic & medicinal chemistry, 10(10), 3145-3151 (2002-08-02)
A series of 3'-N-acyl-paclitaxel analogues 1a-v were synthesized and their cytotoxicities in vitro against several human tumor cell lines examined. It has been shown that distinct correlation between activity and N-acyl-substituent. The appropriate size of N-acyl group was indispensable for
Ester derivatives from tannase-treated prunioside A and their anti-inflammatory activities.
Jun C, et al.
Bull. Korean Chem. Soc., 28(1), 73-73 (2007)

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