Cas 375367-28-5,(2R,3R)-3-[(E)-3-((2S,4S,5R)-3,4-Dimethyl-2-oxo-5-phenyl-2λ<sup>5</sup>-[1,3,2]oxazaphospholidin-2-yl)-allyl]-2-pent-2-ynyl-cyclopentanone

375367-28-5

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Basic information

Product Name: (2R,3R)-3-[(E)-3-((2S,4S,5R)-3,4-Dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yl)-allyl]-2-pent-2-ynyl-cyclopentanone
Synonyms: (2R,3R)-3-[(E)-3-((2S,4S,5R)-3,4-Dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yl)-allyl]-2-pent-2-ynyl-cyclopentanone
CAS NO:375367-28-5
Molecular Formula:
Molecular Weight: 399.47
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3R)-3-[(E)-3-((2S,4S,5R)-3,4-Dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yl)-allyl]-2-pent-2-ynyl-cyclopentanone(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-3-[(E)-3-((2S,4S,5R)-3,4-Dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yl)-allyl]-2-pent-2-ynyl-cyclopentanone(375367-28-5)
EPA Substance Registry System: (2R,3R)-3-[(E)-3-((2S,4S,5R)-3,4-Dimethyl-2-oxo-5-phenyl-2λ⁵-[1,3,2]oxazaphospholidin-2-yl)-allyl]-2-pent-2-ynyl-cyclopentanone(375367-28-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 375367-28-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 375367-28-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,5,3,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 375367-28:
(8*3)+(7*7)+(6*5)+(5*3)+(4*6)+(3*7)+(2*2)+(1*8)=175
175 % 10 = 5
So 375367-28-5 is a valid CAS Registry Number.

375367-28-5Upstream product

375367-28-5Downstream Products

1211-29-6 Methyl jasmonate

375367-28-5Relevant academic research and scientific papers

1,4-Addition of chiral 2-propenylphosphonamide anions to α-substituted cyclopentenones: Use in enantioselective syntheses of methyl dihydrojasmonates and methyl jasmonates

Hailes, Helen C.,Isaac, Ben,Javaid

, p. 7325 - 7328 (2001)

The addition of chiral 2-propenylphosphonamide anions, generated from the reaction products of (1R,2S)-ephedrine and 2-propene-1-phosphonyl dichloride, to α-substituted cyclopentenones is described. Ozonolysis of the addition products led to the synthesis of both enantiomers of methyl dihydrojasmonate and methyl jasmonate.

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