152090-71-6

• 

• Basic information

  1. Product Name: Ethanone, 1-[1-(2-propenyl)cyclopentyl]- (9CI)
  2. Synonyms: Ethanone, 1-[1-(2-propenyl)cyclopentyl]- (9CI)
  3. CAS NO:152090-71-6
  4. Molecular Formula: C10H16O
  5. Molecular Weight: 152.23344
  6. EINECS: N/A
  7. Product Categories: ACETYLGROUP
  8. Mol File: 152090-71-6.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Ethanone, 1-[1-(2-propenyl)cyclopentyl]- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Ethanone, 1-[1-(2-propenyl)cyclopentyl]- (9CI)(152090-71-6)
  11. EPA Substance Registry System: Ethanone, 1-[1-(2-propenyl)cyclopentyl]- (9CI)(152090-71-6)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 152090-71-6(Hazardous Substances Data)

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152090-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152090-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,0,9 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 152090-71:
(8*1)+(7*5)+(6*2)+(5*0)+(4*9)+(3*0)+(2*7)+(1*1)=106
106 % 10 = 6
So 152090-71-6 is a valid CAS Registry Number.

152090-71-6Upstream product

• 153579-96-5 methyl 1-allylcyclopentane-1-carboxylate 
• 411238-08-9 1-(3-propenyl)cyclopentanecarboxylic acid 
• 917-54-4 methyllithium 
• 3400-45-1 cyclopentanecarboxylic acid 
• 75-77-4 chloro-trimethyl-silane 

152090-71-6Downstream Products

• 152090-38-5 1-Acetyl-1-(2-oxoethyl)cyclopentane 

152090-71-6Relevant articles and documents

Palladium-Catalyzed Alkene Carboalkoxylation Reactions of Phenols and Alcohols for the Synthesis of Carbocycles

White, Derick R.,Herman, Madeline I.,Wolfe, John P.

, p. 4311 - 4314 (2017/08/23)

Intermolecular alkene difunctionalization reactions between terminal alkenes bearing a pendant aryl or alkenyl triflate electrophile and exogenous alcohol or phenol nucleophiles are described. These transformations afford substituted indanyl or alkylidene

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