183606-89-5

• 

• Basic information

  1. Product Name: Carbamic acid, (2-oxo-3-cyclopenten-1-yl)-, 1,1-dimethylethyl ester, (S)- (9CI)
  2. Synonyms: Carbamic acid, (2-oxo-3-cyclopenten-1-yl)-, 1,1-dimethylethyl ester, (S)- (9CI)
  3. CAS NO:183606-89-5
  4. Molecular Formula: C10H15NO3
  5. Molecular Weight: 197.231
  6. EINECS: N/A
  7. Product Categories: N-BOC
  8. Mol File: 183606-89-5.mol
  9. Article Data: 1

• 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: Carbamic acid, (2-oxo-3-cyclopenten-1-yl)-, 1,1-dimethylethyl ester, (S)- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: Carbamic acid, (2-oxo-3-cyclopenten-1-yl)-, 1,1-dimethylethyl ester, (S)- (9CI)(183606-89-5)
  11. EPA Substance Registry System: Carbamic acid, (2-oxo-3-cyclopenten-1-yl)-, 1,1-dimethylethyl ester, (S)- (9CI)(183606-89-5)

• 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: 183606-89-5(Hazardous Substances Data)

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183606-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183606-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,6,0 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 183606-89:
(8*1)+(7*8)+(6*3)+(5*6)+(4*0)+(3*6)+(2*8)+(1*9)=155
155 % 10 = 5
So 183606-89-5 is a valid CAS Registry Number.

183606-89-5Upstream product

• 160141-86-6 (S)-methyl 2-(tert-butoxycarbonylamino)-4-(methylsulfonyl)butanoate 
• 183606-80-6 ((S)-1,1,3-Trioxo-hexahydro-1λ⁶-thiopyran-4-yl)-carbamic acid tert-butyl ester 
• 33900-24-2 N-(tert-butoxycarbonyl)-L-methionine methyl ester 

183606-89-5Downstream Products

• 145106-46-3 (S)-N-tert-butoxycarbonyl-2-aminocyclopentanone 

183606-89-5Relevant articles and documents

Amino acid derived thiane oxide and dioxide systems as disposable templates: Synthesis of α-amino ketones, anti-amino alcohols and an amino cyclopentenone

Gamble, Mark P.,Giblin, Gerard M. P.,Montana, John G.,O'Brien, Peter,Ockendon, Timothy P.,Taylor, Richard J. K.

, p. 7457 - 7460 (2007/10/03)

Sulfones and sulfoxides synthesised from methionine and homocysteine thiolactone have been cyclised to amino ketones using potassium bis(trimethylsilyl)amide. Ramberg-Backlund chemistry on one of the sulfones gave an amino cyclopentenone whereas acyclic α-amino ketones and anti-amino alcohols were obtained by Raney nickel desulfurisation of the sulfoxides.

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