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Documentos

328367

Sigma-Aldrich

1-Cyclohexene-1-carboxylic acid

97%

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About This Item

Fórmula lineal:
C6H9CO2H
Número de CAS:
636-82-8
Peso molecular:
126.15
MDL number:
MFCD00001545
UNSPSC Code:
12352100
PubChem Substance ID:
24859731
NACRES:
NA.22

Quality Level

100

assay

97%

form

solid

bp

133-135 °C/14 mmHg (lit.)

mp

35-39 °C (lit.)

density

1.101 g/mL at 25 °C (lit.)

SMILES string

OC(=O)C1=CCCCC1

InChI

1S/C7H10O2/c8-7(9)6-4-2-1-3-5-6/h4H,1-3,5H2,(H,8,9)

InChI key

NMEZJSDUZQOPFE-UHFFFAOYSA-N

Categorías relacionadas

General description

1-Cyclohexene-1-carboxylic acid was identified as intermediate during the anaerobic decomposition of benzoic acid by a methanogenic consortium.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

C102652

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Sigma-Aldrich

108464

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Sigma-Aldrich

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Mariana G de Oliveira et al.
American journal of physiology. Renal physiology, 315(3), F460-F468 (2018-05-03)
Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) is a chronic inflammatory disease without consistently effective treatment. We investigate the role of toll-like receptor 4 (TLR4) on voiding dysfunction and inflammation in the cyclophosphamide (CYP)-induced mouse cystitis. Male C57BL/6 [wild-type, (WT)] and/or TLR4
Xin Xie et al.
Carbohydrate polymers, 225, 115223-115223 (2019-09-16)
A polysaccharide isolated from Strongylocentrotus nudus eggs (SEP) reportedly displays immune activity in vivo. Here, its effect and underlying mechanism in the treatment of pancreatic cancer were investigated. SEP obviously inhibited pancreatic cancer growth by activating NK cells in vitro/vivo
K A Reynolds et al.
Journal of bacteriology, 174(12), 3850-3854 (1992-06-01)
A novel NADPH-dependent enoyl reductase, catalyzing the conversion of 1-cyclohexenylcarbonyl coenzyme A (1-cyclohexenylcarbonyl-CoA) to cyclohexylcarbonyl-CoA, was purified to homogeneity from Streptomyces collinus. This enzyme, a dimer with subunits of identical M(r) (36,000), exhibits a Km of 1.5 +/- 0.3 microM
C L Keith et al.
Archives of microbiology, 118(2), 173-176 (1978-08-01)
A possible pathway for the anaerobic utilization of benzoic acid by a methanogenic consortium is suggested. Cyclohexane carboxylic acid and 1-cyclohexene-1-carboxylic acid have been identified as intermediates before ring rupture. Suprisingly, 3-cyclohexene-1-carboxylic acid interferes with utilization of other cyclic acids.
M S Elshahed et al.
Applied and environmental microbiology, 67(4), 1728-1738 (2001-04-03)
The metabolism of benzoate, cyclohex-1-ene carboxylate, and cyclohexane carboxylate by "Syntrophus aciditrophicus" in cocultures with hydrogen-using microorganisms was studied. Cyclohexane carboxylate, cyclohex-1-ene carboxylate, pimelate, and glutarate (or their coenzyme A [CoA] derivatives) transiently accumulated during growth with benzoate. Identification was
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