107866-66-0

• 

• Basic information

  1. Product Name: (E)-(S)-1-((R)-Toluene-4-sulfinyl)-non-3-en-2-ol
  2. Synonyms: (E)-(S)-1-((R)-Toluene-4-sulfinyl)-non-3-en-2-ol
  3. CAS NO:107866-66-0
  4. Molecular Formula:
  5. Molecular Weight: 280.431
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 107866-66-0.mol
  9. Article Data: 2

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: (E)-(S)-1-((R)-Toluene-4-sulfinyl)-non-3-en-2-ol(CAS DataBase Reference)
  10. NIST Chemistry Reference: (E)-(S)-1-((R)-Toluene-4-sulfinyl)-non-3-en-2-ol(107866-66-0)
  11. EPA Substance Registry System: (E)-(S)-1-((R)-Toluene-4-sulfinyl)-non-3-en-2-ol(107866-66-0)

• 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: 107866-66-0(Hazardous Substances Data)

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107866-66-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107866-66-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,6 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107866-66:
(8*1)+(7*0)+(6*7)+(5*8)+(4*6)+(3*6)+(2*6)+(1*6)=150
150 % 10 = 0
So 107866-66-0 is a valid CAS Registry Number.

107866-66-0Upstream product

• 1519-39-7 (R)-methyl p-tolyl sulfoxide 
• 2351-90-8 ethyl (2E)-oct-2-enoate 
• 107866-63-7 (E)-1-((R)-Toluene-4-sulfinyl)-non-3-en-2-one 

107866-66-0Downstream Products

• 116885-47-3 p-tolylsulfonyl 3-nonene 2-ol 
• 116949-51-0 p-tolylsulfonyl 3,4-epoxy 2-nonanol, threo 
• 116885-46-2 p-tolylsulfonyl 3,4-epoxy 2-nonanol, erythro 

107866-66-0Relevant articles and documents

Stereospecific hydroxylation of chiral allylic β-hydroxysulfoxides: asymmetric synthesis of L-arabinitol

Solladie, Guy,Frechou, Catherine,Hutt, Jean,Demailly, Gilles

, p. 827 - 836 (2007/10/02)

Chiral allylic β-hydroxysulfoxides 2 have been hydroxylated by the osmium tetroxide catalyzed reaction.The reaction can be highly stereoselective depending on the nature of the substituent linked to the double bond and the configurations of the sulfoxide and hydroxylic groups.The diastereoselectivity can be as high as 90 percent.This methodology was applied to the asymmetric synthesis of L-arabinitol.

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