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BOC-HYP-OH

Product Name
BOC-HYP-OH
CAS No.
331442-12-7
Chemical Name
BOC-HYP-OH
Synonyms
BOC-L-HYP-OH;BOC-TRANS-HYP-OH;BOC-HYDROXYPROLINE;RARECHEM EM WB 0136;BOC-L-4-HYDROXYPROLINE;N-BOC-L-4-HYDROXYPROLINE;BOC-L-T-4-HYDROXYPROLINE;N-BOC-4-HYDROXY-L-PROLINE;BOC-L-TRANS-4-HYDROXYPROLINE;BOC-TRANS-4-HYDROXY-L-PROLINE
CBNumber
CB8411794
Molecular Formula
C10H17NO5
Formula Weight
231.25
MOL File
331442-12-7.mol
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BOC-HYP-OH Property

Melting point:
123-127 °C(lit.)
Boiling point:
390.9±42.0 °C(Predicted)
Density 
1.312±0.06 g/cm3(Predicted)
storage temp. 
−20°C
pka
3.80±0.40(Predicted)
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Safety

Safety Statements 
22-24/25
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

BOC-HYP-OH Preparation Products And Raw materials

Raw materials

Preparation Products

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BOC-HYP-OH Suppliers

Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63711
Advantage
58

331442-12-7, BOC-HYP-OHRelated Search:


  • RARECHEM EM WB 0136
  • N-BOC-TRANS-4-HYDROXY-L-PROLINE
  • N-BOC-L-TRANS-4-HYDROXYPROLINE
  • N-BOC-L-4-HYDROXYPROLINE
  • N-BOC-4-HYDROXY-L-PROLINE
  • N-ALPHA-T-BUTOXYCARBONYL-TRANS-4-HYDROXY-L-PROLINE
  • N-ALPHA-TERT-BUTYLOXYCARBONYL-L-4-HYDROXYPROLINE
  • N-ALPHA-T-BOC-L-TRANS-4-HYDROXYPROLINE
  • N-ALPHA-T-BOC-L-HYDROXYPROLINE
  • N-ALPHA-T-BOC-TRANS-4-HYDROXY-L-PROLINE
  • N-ALPHA-T-BUTOXYCARBONYL-L-HYDROXYPROLINE
  • N-TERT-BUTOXYCARBONYL-L-HYDROXYPROLINE
  • N-(TERT-BUTOXYCARBONYL)-L-4-HYDROXYPROLINE
  • N-T-BOC-TRANS-4-HYDROXY-L-PROLINE
  • BOC-(2S,4R)-(-)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID
  • BOC-HYDROXYPROLINE
  • BOC-L-4-HYDROXYPROLINE
  • BOC-L-HYP-OH
  • BOC-TRANS-4-HYDROXY-L-PROLINE
  • BOC-TRANS-HYP-OH
  • BOC-L-TRANS-4-HYDROXYPROLINE
  • BOC-L-T-4-HYDROXYPROLINE
  • (2S,4R)-N-ALPHA-T-BUTOXYCARBONYL-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID
  • 1,2-Pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-dimethylethyl) ester, (2S)-
  • 331442-12-7
  • Boc-Amino Acids
  • Amino Acids (N-Protected)
  • Protected & Labeled Amino Acids
  • Unnatural Amino Acid Derivatives
  • Specialty Synthesis
  • Proline Derivatives
  • Peptide Synthesis