112283-40-6

• 

• Basic information

  1. Product Name: 1-Azabicyclo[3.2.0]heptane-2-carboxylicacid,7-oxo-,(2R,5R)-(9CI)
  2. Synonyms: 1-Azabicyclo[3.2.0]heptane-2-carboxylicacid,7-oxo-,(2R,5R)-(9CI)
  3. CAS NO:112283-40-6
  4. Molecular Formula: C7H9NO3
  5. Molecular Weight: 155.15
  6. EINECS: N/A
  7. Product Categories: CARBOXYLICACID;PYRROLE
  8. Mol File: 112283-40-6.mol
  9. Article Data: 4

• 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: 1-Azabicyclo[3.2.0]heptane-2-carboxylicacid,7-oxo-,(2R,5R)-(9CI)(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1-Azabicyclo[3.2.0]heptane-2-carboxylicacid,7-oxo-,(2R,5R)-(9CI)(112283-40-6)
  11. EPA Substance Registry System: 1-Azabicyclo[3.2.0]heptane-2-carboxylicacid,7-oxo-,(2R,5R)-(9CI)(112283-40-6)

• 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: 112283-40-6(Hazardous Substances Data)

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112283-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112283-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112283-40:
(8*1)+(7*1)+(6*2)+(5*2)+(4*8)+(3*3)+(2*4)+(1*0)=86
86 % 10 = 6
So 112283-40-6 is a valid CAS Registry Number.

112283-40-6Upstream product

• 112419-10-0 (3S,5S)-carbapenam 
• 176036-37-6 (2S,5S)-trans-5-carboxymethylproline 
• 64199-88-8 Δ¹-pyrroline-5-carboxylic acid 
• 56-86-0 L-glutamic acid 
• 64-19-7 acetic acid 

112283-40-6Downstream Products

112283-40-6Relevant articles and documents

Carboxymethylproline synthase catalysed syntheses of functionalised N-heterocycles

Hamed, Refaat B.,Mecinovic, Jasmin,Ducho, Christian,Claridge, Timothy D. W.,Schofield, Christopher J.

, p. 1413 - 1415 (2010)

The utility of wild-type and variant carboxymethylproline synthases for biocatalysis was demonstrated by preparing functionalised 5-, 6- and 7-membered N-heterocycles from amino acid aldehydes and (alkylated) malonyl-coenzyme A derivatives; the N-heterocycles produced were converted to the corresponding bicyclic β-lactams by a carbapenem synthetase. The Royal Society of Chemistry 2010.

Three unusual reactions mediate carbapenem and carbapenam biosynthesis [1]

Li, Rongfeng,Stapon, Anthony,Blanchfield, Joanne T.,Townsend, Craig A.

, p. 9296 - 9297 (2000)

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