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3-Cyclohexenecarboxylic acid

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3-Cyclohexenecarboxylic acid Basic information

Product Name:
3-Cyclohexenecarboxylic acid
Synonyms:
  • CYCLOHEX-3-ENE-1-CARBOXYLIC ACID
  • CYCLOHEX-3-ENECARBOXYLIC ACID
  • 1,2,3,6-TETRAHYDROBENZOIC ACID
  • 3-Cyclohexenecarboxy
  • 3-Cyclohexene-1-carboxylic acid 97%
  • 3-ringhasene-1-forMicacid
  • 3 - cyclohexene - 1 - forMic acid
  • Cyclohex-3-ene-1-carboxylic acid 98%
CAS:
4771-80-6
MF:
C7H10O2
MW:
126.15
EINECS:
225-314-7
Product Categories:
  • Carboxylic Acids
  • Ring Systems
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • pharmacetical
  • Carboxylic Acids
  • heterocyclic/Aliphatic series
  • bc0001
Mol File:
4771-80-6.mol
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3-Cyclohexenecarboxylic acid Chemical Properties

Melting point:
17 °C (lit.)
Boiling point:
130-133 °C/4 mmHg (lit.)
Density 
1.081 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.48(lit.)
Flash point:
230 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
Liquid
pka
4.67±0.20(Predicted)
Specific Gravity
1.08
color 
Clear yellow-brownish to gray-bluish
Water Solubility 
insoluble
BRN 
1617723
Stability:
Stable. Combustible. Incompatible with bases, strong oxidizing agents.
InChIKey
VUSWCWPCANWBFG-UHFFFAOYSA-N
CAS DataBase Reference
4771-80-6(CAS DataBase Reference)
NIST Chemistry Reference
3-Cyclohexene-1-carboxylic acid(4771-80-6)
EPA Substance Registry System
3-Cyclohexene-1-carboxylic acid (4771-80-6)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
21-34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
RTECS 
GW3675000
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29162090

MSDS

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3-Cyclohexenecarboxylic acid Usage And Synthesis

Chemical Properties

colourless liquid

Uses

3-Cyclohexenylcarboxylic Acid has been found to be an oxidizable, nongrowth substrate and induces the metabolism of cyclohexanecarboxylic acid and benzoic acid in a strain of Pseudomonas putida. 3-Cyclohexenylcarboxylic Acid has been used as food for cultures of Streptomyces sp. ??KCTC 11604BP fkbO deletion mutant to make 32-dehydroxy-FK506, a FK506 analogue containing a non-natural starter unit.

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