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C116602

Sigma-Aldrich

Cyclopropanecarboxylic acid

95%

Sinonimo/i:

CPC-acid

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About This Item

Formula condensata:
C3H5CO2H
Numero CAS:
1759-53-1
Peso molecolare:
86.09
Beilstein:
969839
Numero CE:
217-162-5
Numero MDL:
MFCD00001287
Codice UNSPSC:
12352100
ID PubChem:
24892369
NACRES:
NA.22

Livello qualitativo

100

Saggio

95%

Stato

liquid

Indice di rifrazione

n20/D 1.438 (lit.)

P. ebollizione

182-184 °C (lit.)

Punto di fusione

14-17 °C (lit.)

Densità

1.081 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

OC(=O)C1CC1

InChI

1S/C4H6O2/c5-4(6)3-1-2-3/h3H,1-2H2,(H,5,6)
YMGUBTXCNDTFJI-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

Corrosion
GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314

Classi di pericolo

Skin Corr. 1B

Codice della classe di stoccaggio

8A - Combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

161.6 °F - closed cup

Punto d’infiammabilità (°C)

72 °C - closed cup

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
STBL0330
13225KSV
STBB9094V
S42644
S39991

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Sigma-Aldrich

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Sigma-Aldrich

209759

2-Methylcyclopropanecarboxylic acid

Cyclopropanemethanol ≥99.5%

Sigma-Aldrich

482099

Cyclopropanemethanol

CYCLOPROPANECARBOXAMIDE AldrichCPR

S455989

CYCLOPROPANECARBOXAMIDE

4-Chlorobutyronitrile 97%

Sigma-Aldrich

C30000

4-Chlorobutyronitrile

Makoto Shiozaki et al.
Bioorganic & medicinal chemistry letters, 19(21), 6213-6217 (2009-09-22)
A series of 1-sulfonylaminocyclopropanecarboxylates was synthesized as ADAMTS-5 (Aggrecanase-2) inhibitors. After an intensive investigation of the central cyclopropane core including its absolute stereochemistry and substituents, we found compound 22 with an Agg-2 IC50=7.4 nM, the most potent ADAMTS-5 inhibitor reported
G B Quistad et al.
Drug metabolism and disposition: the biological fate of chemicals, 14(5), 521-525 (1986-09-01)
Conjugation with carnitine is a major metabolic pathway for cyclopropanecarboxylic acid (CPCA). The CPCA-carnitine is cleaved enzymatically (carnitine acetyltransferase) more slowly in vitro than are acetyl- and propionylcarnitines, but also slightly more extensively. When given orally to a rat, CPCA-carnitine
Dan Yang et al.
The Journal of organic chemistry, 75(14), 4796-4805 (2010-06-24)
The monomer 1 derived from achiral 1-(aminoxy)cyclopropanecarboxylic acid (OAcc) and oligopeptides 2-9 consisting of a chiral alpha-aminoxy acid and an achiral alpha-aminoxy acid such as OAcc were synthesized and their structures characterized. The eight-membered-ring intramolecular hydrogen bond, namely the alpha
Ying Yao et al.
The Journal of organic chemistry, 76(8), 2807-2813 (2011-03-19)
Highly effective asymmetric hydrogenation of protected ethyl 1-(2-aminoaceto)cyclopropane carboxylates in the presence of [RuCl(benzene)(S)-SunPhos]Cl was realized, and high enantioselectivities (up to 98.7% ee) were obtained. This asymmetric hydrogenation provides a key intermediate for the enantioselective synthesis of (S)-7-amino-5-azaspiro[2.4]heptane moiety of
S Shuto et al.
Journal of medicinal chemistry, 39(24), 4844-4852 (1996-11-22)
We recently demonstrated that (+/-)-(Z)-2-(aminomethyl)-1-phenyl-N,N-diethylcyclopropanecarboxamide [milnacipran, (+/-)-1], an inhibitor of the reuptake of serotonin (5-HT), was a noncompetitive NMDA receptor antagonist. On the basis of the cyclopropane structure of (+/-)-1, conformationally restricted analogs with different stereochemistries, namely 1-phenyl-2-(1-aminoalkyl)-N,N-diethylcyclopropanecarboxamindes (2, 3
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