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453757

Sigma-Aldrich

3-Cyclohexene-1-carboxylic acid

97%

동의어(들):

1,2,3,6-Tetrahydrobenzoic acid

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About This Item

Linear Formula:
C6H9CO2H
CAS Number:
4771-80-6
Molecular Weight:
126.15
EC Number:
225-314-7
MDL number:
MFCD00013781
UNSPSC 코드:
12352100
PubChem Substance ID:
24868850
NACRES:
NA.22

Quality Level

100

분석

97%

refractive index

n20/D 1.48 (lit.)

bp

130-133 °C/4 mmHg (lit.)

mp

17 °C (lit.)

density

1.081 g/mL at 25 °C (lit.)

작용기

carboxylic acid

SMILES string

OC(=O)C1CCC=CC1

InChI

1S/C7H10O2/c8-7(9)6-4-2-1-3-5-6/h1-2,6H,3-5H2,(H,8,9)

InChI key

VUSWCWPCANWBFG-UHFFFAOYSA-N

유사한 제품을 찾으십니까? 방문 제품 비교 안내

관련 카테고리

픽토그램

CorrosionExclamation mark
GHS05,GHS07

신호어

Danger

유해 및 위험 성명서

H312,H314

Hazard Classifications

Acute Tox. 4 Dermal - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point (°F)

230.0 °F - closed cup

Flash Point (°C)

110 °C - closed cup

개인 보호 장비

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

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시험 성적서(COA)

Lot/Batch Number
STBG5555V
S43576V
S43576
04520JE
S37073

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특정 버전이 필요한 경우 로트 번호나 배치 번호로 특정 인증서를 찾을 수 있습니다.

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문서 라이브러리 방문

E R Blakley et al.
Canadian journal of microbiology, 28(12), 1324-1329 (1982-12-01)
A strain of Pseudomonas putida grew rapidly on cyclohexanecarboxylic acid as a sole source of carbon. A CoA-mediated beta-oxidation pathway was induced for the metabolism of the compound. The organism could not utilize 3-cyclohexenecarboxylic acid as a sole source of
Karine Barral et al.
Journal of medicinal chemistry, 48(2), 450-456 (2005-01-22)
Starting from commercially available (rac)-3-cyclohexene-1-carboxylic acid, a series of purine and pyrimidine cis-substituted cyclohexenyl and cyclohexanyl nucleosides were synthesized through a key Mitsunobu reaction. Antiviral evaluations were performed on HIV, coxsackie B3, and herpes viruses (HSV-1, HSV-2, VZV, HCMV). Three
Bromination of 3-cyclohexene-1-carboxylic acid, epoxydation of methyl 3-cyclohexene-1-carboxylate and opening of methyl cis-and trans-3, 4-epoxycyclohexane-1-carboxylate: Stereochemical results.
Bellucci G, et al.
Tetrahedron, 28(13), 3393-3399 (1972)
Yi Yang et al.
Environmental science & technology, 48(4), 2344-2351 (2014-02-01)
The effect of halides on organic contaminant destruction efficiency was compared for UV/H2O2 and UV/S2O8(2-) AOP treatments of saline waters; benzoic acid, 3-cyclohexene-1-carboxylic acid, and cyclohexanecarboxylic acid were used as models for aromatic, alkene, and alkane constituents of naphthenic acids
Total synthesis of (.+-.)-methyl shikimate and (.+-.)-3-phosphoshikimic acid.
Bartlett PA and McQuaid LA.
Journal of the American Chemical Society, 106(25), 7854-7860 (1984)
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