Boc-D-Phe-Pro-OH

Modify Date: 2024-01-02 13:12:52

Boc-D-Phe-Pro-OH Structure
Boc-D-Phe-Pro-OH structure
 Common Name Boc-D-Phe-Pro-OH
CAS Number 38675-10-4 Molecular Weight 362.420
Density 1.2±0.1 g/cm3 Boiling Point 594.4±50.0 °C at 760 mmHg
Molecular Formula C19H26N2O5 Melting Point N/A
MSDS N/A Flash Point 313.3±30.1 °C

 Names

Name boc-d-phe-pro-oh
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 594.4±50.0 °C at 760 mmHg
Molecular Formula C19H26N2O5
Molecular Weight 362.420
Flash Point 313.3±30.1 °C
Exact Mass 362.184174
PSA 95.94000
LogP 2.75
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.555
Storage condition 2-8°C

 Safety Information

Hazard Codes Xi

 Synthetic Route

(S)-benzyl 1-((R)-2-(tert-butoxycarbonylamino)-3-phenylpropanoyl)pyrrolidine-2-carboxylate structure

(S)-benzyl 1-((...

CAS#:64471-88-1

~86%

Boc-D-Phe-Pro-OH Structure

Boc-D-Phe-Pro-OH

CAS#:38675-10-4

Literature: Oleksyszyn, Jozef; Boduszek, Bogdan; Kam, Chih-Min; Powers, James C. Journal of Medicinal Chemistry, 1994 , vol. 37, # 2 p. 226 - 231
Boc-D-Phe-OH structure

Boc-D-Phe-OH

CAS#:18942-49-9

~%

Boc-D-Phe-Pro-OH Structure

Boc-D-Phe-Pro-OH

CAS#:38675-10-4

Literature: Das, Jagabandhu; Kimball; Hall, Steven E.; Han, Wen-Ching; Iwanowicz, Edwin; Lin, James; Moquin, Robert V.; Reid, Joyce A.; Sack, John S.; Malley, Mary F.; Chang, Chiehying Y.; Chong, Saeho; Wang-Iverson, David B.; Roberts, Daniel G.M.; Seiler, Steven M.; Schumacher, William A.; Ogletree, Martin L. Bioorganic and Medicinal Chemistry Letters, 2002 , vol. 12, # 1 p. 45 - 49
N/A structure

N/A

CAS#:126251-09-0

~%

Boc-D-Phe-Pro-OH Structure

Boc-D-Phe-Pro-OH

CAS#:38675-10-4

Literature: Poplawski, Sarah E.; Lai, Jack H.; Sanford, David G.; Sudmeier, James L.; Wu, Wengen; Bachovchin, William W. Journal of Medicinal Chemistry, 2011 , vol. 54, # 7 p. 2022 - 2028
H-Pro-OBzl.HCl structure

H-Pro-OBzl.HCl

CAS#:16652-71-4

~%

Boc-D-Phe-Pro-OH Structure

Boc-D-Phe-Pro-OH

CAS#:38675-10-4

Literature: Costanzo, Michael J.; Almond Jr., Harold R.; Hecker, Leonard R.; Schott, Mary R.; Yabut, Stephen C.; Zhang, Han-Cheng; Andrade-Gordon, Patricia; Corcoran, Thomas W.; Giardino, Edward C.; Kauffman, Jack A.; Lewis, Joan M.; De Garavilla, Lawrence; Haertlein, Barbara J.; Maryanoff, Bruce E. Journal of Medicinal Chemistry, 2005 , vol. 48, # 6 p. 1984 - 2008
methyl 2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoate structure

methyl 2-[(2-me...

CAS#:19901-50-9

~%

Boc-D-Phe-Pro-OH Structure

Boc-D-Phe-Pro-OH

CAS#:38675-10-4

Literature: Horton, Alexandra E.; May, Oliver S.; Elsegood, Mark R. J.; Kimber, Marc C. Synlett, 2011 , # 6 p. 797 - 800
L-Proline, phenylmethylester structure

L-Proline, phen...

CAS#:41324-66-7

~%

Boc-D-Phe-Pro-OH Structure

Boc-D-Phe-Pro-OH

CAS#:38675-10-4

Literature: Das, Jagabandhu; Kimball; Hall, Steven E.; Han, Wen-Ching; Iwanowicz, Edwin; Lin, James; Moquin, Robert V.; Reid, Joyce A.; Sack, John S.; Malley, Mary F.; Chang, Chiehying Y.; Chong, Saeho; Wang-Iverson, David B.; Roberts, Daniel G.M.; Seiler, Steven M.; Schumacher, William A.; Ogletree, Martin L. Bioorganic and Medicinal Chemistry Letters, 2002 , vol. 12, # 1 p. 45 - 49

 Synonyms

BOC-N-Me-D-Phe-Pro
N-(tert-Butoxycarbonyl)-D-phenylalanyl-L-proline
BOC-D-PHE-L-PRO-OH
L-Proline, N-[(1,1-dimethylethoxy)carbonyl]-D-phenylalanyl-
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-D-phenylalanyl-L-proline
N-tert-butoxycarbonyl-D-phenylalanyl-L-proline
tert-butyloxycarbonyl-D-phenylalanyl-L-proline
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