110452-53-4

• 

• Basic information

  1. Product Name: D-Proline, 5-(1-methylethyl)-, cis- (9CI)
  2. Synonyms: D-Proline, 5-(1-methylethyl)-, cis- (9CI)
  3. CAS NO:110452-53-4
  4. Molecular Formula: C8H15NO2
  5. Molecular Weight: 157.2102
  6. EINECS: N/A
  7. Product Categories: PYRROLE;ISOPROPYL
  8. Mol File: 110452-53-4.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: D-Proline, 5-(1-methylethyl)-, cis- (9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: D-Proline, 5-(1-methylethyl)-, cis- (9CI)(110452-53-4)
  11. EPA Substance Registry System: D-Proline, 5-(1-methylethyl)-, cis- (9CI)(110452-53-4)

• 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: 110452-53-4(Hazardous Substances Data)

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110452-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110452-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,4,5 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110452-53:
(8*1)+(7*1)+(6*0)+(5*4)+(4*5)+(3*2)+(2*5)+(1*3)=74
74 % 10 = 4
So 110452-53-4 is a valid CAS Registry Number.

110452-53-4Upstream product

• 1071227-06-9 [4S,6S,8aS]-6-isopropyl-4-phenyl-hexahydropyrrolo[2,1-c]-[1,4]oxazin-1-one 

110452-53-4Downstream Products

110452-53-4Relevant articles and documents

Short enantioselective syntheses of trans-5-alkylprolines from new functionalized amino alcohols

Alladoum, Jeanne,Roland, Sylvain,Vrancken, Emmanuel,Mangeney, Pierre,Kadouri-Puchot, Catherine

experimental part, p. 9771 - 9774 (2009/04/06)

(Chemical Equation Presented) Amino alcohols, having an enol ether function, cyclized in acidic medium to give quantitatively diastereosomerically pure bicyclic compounds that were transformed in five steps in enantiopure trans-5-alkylproline derivatives.

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