166583-62-6

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• Basic information

  1. Product Name: 1-Cyclohexene-1-carboxaldehyde,3-hydroxy-4-(1-methylethyl)-,(3S,4R)-(9CI)
  2. Synonyms: 1-Cyclohexene-1-carboxaldehyde,3-hydroxy-4-(1-methylethyl)-,(3S,4R)-(9CI)
  3. CAS NO:166583-62-6
  4. Molecular Formula: C10H16O2
  5. Molecular Weight: 168.23
  6. EINECS: N/A
  7. Product Categories: ISOPROPYL
  8. Mol File: 166583-62-6.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 281.6±40.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 1.096±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. PKA: 14.34±0.60(Predicted)
  10. CAS DataBase Reference: 1-Cyclohexene-1-carboxaldehyde,3-hydroxy-4-(1-methylethyl)-,(3S,4R)-(9CI)(CAS DataBase Reference)
  11. NIST Chemistry Reference: 1-Cyclohexene-1-carboxaldehyde,3-hydroxy-4-(1-methylethyl)-,(3S,4R)-(9CI)(166583-62-6)
  12. EPA Substance Registry System: 1-Cyclohexene-1-carboxaldehyde,3-hydroxy-4-(1-methylethyl)-,(3S,4R)-(9CI)(166583-62-6)

• 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: 166583-62-6(Hazardous Substances Data)

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166583-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166583-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,5,8 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 166583-62:
(8*1)+(7*6)+(6*6)+(5*5)+(4*8)+(3*3)+(2*6)+(1*2)=166
166 % 10 = 6
So 166583-62-6 is a valid CAS Registry Number.

166583-62-6Upstream product

• 23963-70-4 (S)-4-Isopropyl-cyclohex-1-enecarbaldehyde 
• 18031-40-8 (S)-(-)-perillaldehyde 
• 2158-59-0 cryptone 
• 147729-85-9 2α-isopropyl-8-oxabicyclo[3.2.1]oct-6-ene 

166583-62-6Downstream Products

166583-62-6Relevant articles and documents

Absolute configuration of a new mosquito repellent, (+)-eucamalol and the repellent activity of its epimer.

Satoh,Utamura,Nakade,Nishimura

, p. 1139 - 1141 (2007/10/02)

(+)-Eucamalol (1) and (-)-1-epi-eucamalol (2) were synthesized from (S)-(-)-perillaldehyde to determine the absolute configuration of 1, the structure of natural (+)-eucamalol being determined to be (1R,6R)-(+)-3-formyl-6-isopropyl-2-cyclohexen-1-ol. (+)-

New mosquito repellent from Eucalyptus camaldulensis

Watanabe,Shono,Kakimizu,Okada,Matsuo,Satoh,Nishimura

, p. 2164 - 2166 (2007/10/02)

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