CAS No 6894-38-8 , 2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetic acid

Name: 2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetic acid
Synonyms: CHEBI:18292; 3-Oxo-2-(2-pentenyl)cyclopentaneacetic acid;2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetic acid;(-)-Jasmonic acid; CHEMBL449572; Jasmonate; 6894-38-8;
CAS Registry Number:6894-38-8
Flash Point: 184.6°C
Boiling Point: 358.1°C at 760 mmHg
Density: 1.061g/cm³
Refractive index: 1.49
Flash Point: 184.6°C
EINECS: 213-192-8
Molecular Weight: 210.26952
InchiKey: ZNJFBWYDHIGLCU-HWKXXFMVSA-N
InChI: InChI=1S/C12H18O3/c1-2-3-4-5-10-9(8-12(14)15)6-7-11(10)13/h3-4,9-10H,2,
5-8H2,1H3,(H,14,15)/b4-3-/t9-,10-/m1/s1
Molecular Formula: C₁₂H₁₈O₃
Molecular Structure:

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           6894-38-8 JASMONIC ACID
           
             CHEMOS GmbH
             
              [Manufacturer]
Tel:  0049 9402/9336 0
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Address: CHEMOS GmbH 
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           6894-38-8 JASMONIC ACID-13C1, D2
           
             VARDA Biotech (P) Ltd.
             
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Mumbai-400053, INDIA. null,nullIndia

           6894-38-8 (-)-JASMONIC ACID
           
             Rongkang industry Co.,Ltd
             
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           6894-38-8 (12R)-3-OXO-2-(2Z)-2-PENTENYL-CYCLOPENTANEACETIC ACID
           
             Nanjing Chemlin Chemical Industry Co.,Ltd.
             
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References of 2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetic acid

Title: Jasmonic Acid
CAS Registry Number: 6894-38-8
CAS Name: (1R,2R)-3-Oxo-2-(2Z)-2-penten-ylcyclopentaneacetic acid
Synonyms: (1S,2S)-3-oxo-2-(2￠-cis-pentenyl)cyclopentan-1-acetate; JA
Molecular Formula: C12H18O3
Molecular Weight: 210.27
Percent Composition: C 68.54%, H 8.63%, O 22.83%
Literature References: Naturally occurring plant growth inhibitor. Orginally isolated from jasmin flowers as the methyl ester, the major aroma component: E. Demole et al., Helv. Chim. Acta 45, 675 (1962). Isoln of the free acid from Lasiodiplodia theobromae: D. C. Aldridge et al., J. Chem. Soc. 1971, 1623; by fermentation: D. Broadbent et al., GB 1286266 (1972 to ICI). Occurrence in plants: A. Meyer et al., J. Plant Growth Regul. 3, 1 (1984). NMR characterization: A. Husain et al., J. Nat. Prod. 56, 2008 (1993). Quantification by GC/MS: M. J. Mueller, W. Brodschelm, Anal. Biochem. 218, 425 (1994). Resoln of racemate: R. Kramell et al., Phytochem. Anal. 7, 209 (1996). Review of role in plant development: Y. Koda, Int. Rev. Cytol. 135, 155-199 (1992); of biochemisty and physiology: G. Sembdner, B. Parthier, Annu. Rev. Plant Physiol. Plant Mol. Biol. 44, 569-589 (1993); of signaling in plants: P. Staswick, Curr. Top. Plant Physiol. 11, 14-23 (1993).
Properties: Colorless oil. nD23 1.486. [a]D25 -73° (c = 1 in CH3OH).
Optical Rotation: [a]D25 -73° (c = 1 in CH3OH)
Index of refraction: nD23 1.486

Derivative Type: Methyl ester
CAS Registry Number: 1211-29-6
Synonyms: (-)-Methyl cis-2-pent-2￠-enyl-3-oxocyclopentylacetate; JA-ME; MeJA; methyl jasmonate
Molecular Formula: C13H20O3
Molecular Weight: 224.30
Percent Composition: C 69.61%, H 8.99%, O 21.40%
Properties: Colorless liquid with a sharp persistent odor. nD21.8 1.4730. [a]D -76.5° (c = 3.4 in CH3OH). d422.6 1.021.
Optical Rotation: [a]D -76.5° (c = 3.4 in CH3OH)
Index of refraction: nD21.8 1.4730
Density: d422.6 1.021

Use: Methyl ester in perfumes.