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cis-1-Boc-amino-2-methylcyclopropane-1-carboxylic acid

Base Information
  • Chemical Name:cis-1-Boc-amino-2-methylcyclopropane-1-carboxylic acid
  • CAS No.:88950-65-6
  • Molecular Formula:C10H17NO4
  • Molecular Weight:215.25
  • Hs Code.:
  • DSSTox Substance ID:DTXSID201125354
cis-1-Boc-amino-2-methylcyclopropane-1-carboxylic acid

Synonyms:1535210-05-9;SCHEMBL4643135;DTXSID201125354;AT17016;EN300-7445163;CIS-1-BOC-AMINO-2-METHYLCYCLOPROPANE-1-CARBOXYLIC ACID;rac-(1R,2R)-1-{[(tert-butoxy)carbonyl]amino}-2-methylcyclopropane-1-carboxylic acid;rel-(1R,2R)-1-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-methylcyclopropanecarboxylic acid;88950-65-6

Suppliers and Price of cis-1-Boc-amino-2-methylcyclopropane-1-carboxylic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of cis-1-Boc-amino-2-methylcyclopropane-1-carboxylic acid
Chemical Property:
  • XLogP3:1.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:4
  • Exact Mass:215.11575802
  • Heavy Atom Count:15
  • Complexity:294
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1CC1(C(=O)O)NC(=O)OC(C)(C)C
  • Isomeric SMILES:C[C@@H]1C[C@@]1(C(=O)O)NC(=O)OC(C)(C)C
Technology Process of cis-1-Boc-amino-2-methylcyclopropane-1-carboxylic acid

There total 6 articles about cis-1-Boc-amino-2-methylcyclopropane-1-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydrogencarbonate; In tetrahydrofuran; for 8h; Ambient temperature;
DOI:10.1021/jo00030a009
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