Home Cart Sign in  
Chemical Structure| 132622-78-7 Chemical Structure| 132622-78-7
Chemical Structure| 132622-78-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Synonyms: (4S)-1-Boc-4-amino-D-proline

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of (4S)-1-Boc-4-amino-D-proline

CAS No. :132622-78-7
Formula : C10H18N2O4
M.W : 230.26
SMILES Code : O=C([C@@H]1N(C(OC(C)(C)C)=O)C[C@@H](N)C1)O
Synonyms :
(4S)-1-Boc-4-amino-D-proline
MDL No. :MFCD08704543
InChI Key :WDWRIVZIPSHUOR-NKWVEPMBSA-N
Pubchem ID :14842627

Safety of (4S)-1-Boc-4-amino-D-proline

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of (4S)-1-Boc-4-amino-D-proline

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 132622-78-7 ]

[ 132622-78-7 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 132622-78-7 ]
  • [ 2651-15-2 ]
  • (2R,4S)-4-({Methylsulfanyl-[(E)-toluene-4-sulfonylimino]-methyl}-amino)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester [ No CAS ]
  • 2
  • [ 132622-77-6 ]
  • [ 132622-78-7 ]
  • 3
  • [ 132622-78-7 ]
  • [ 132622-79-8 ]
  • 4
  • [ 77450-00-1 ]
  • [ 132622-78-7 ]
  • 5
  • [ 132623-06-4 ]
  • [ 132622-78-7 ]
  • 6
  • [ 132622-75-4 ]
  • [ 132622-78-7 ]
  • 7
  • trans azido acid [ No CAS ]
  • [ 132622-77-6 ]
  • [ 132622-78-7 ]
YieldReaction ConditionsOperation in experiment
97% EXAMPLE 19 STR21 (4S)-1-(tert-Butoxycarbonyl)-4-amino-D-proline (21). The trans azido acid 20b (2.0 g, 7.81 mmol) was hydrogenated as for the synthesis of 6, to give 2.1 g (97% yield) of 21 containing an equivalent of ethanol (by 1 H NMR), after crystallization from ethanol, m.p.=225-226 C. (decomp.) 1 H NMR (CDCl3) delta 1.42/1.47 (2s, 9H), 2.28 (m, 1H), 2.45 (m, 1H), 3.58 (m, 1H), 3.80 (m, 1H), 3.99 (m, 1H), 4.24 (m, 1H). Anal. after high vacuum at 55 C. for 18 h; (C10 H18 N2 O4.0.25 H2 O) C, H, N.
  • 8
  • [ 132622-78-7 ]
  • (4S)-1-(tert-Butoxycarbonyl)-4-[(p-toluenesulfonyliminoaminomethyl)amino]-D-proline [ No CAS ]
  • (4S)-1-(tert-Butoxycarbonyl)-4-([(p-toluenesulfonyl-iminoaminomethyl)amino]methyl)-L-proline [ No CAS ]
YieldReaction ConditionsOperation in experiment
EXAMPLE 20 STR22 (4S)-1-(tert-Butoxycarbonyl)-4-[(p-toluenesulfonyliminoaminomethyl)amino]-D-proline (22). The amino acid 21 (1.5 g, 5.43 mmol) was converted to 10 using the procedure for the preparation of 13. This gave 600 mg (26% yield) after crystallization from EtOAc/Et2 O/hexane, m.p.=190-191 C. (decomp.). 1 H NMR (d6 DMSO) delta 1.32/1.37 (2s, 9H), 2.05 (m, 2H), 2.35 (s, 3H), 3.04 (m, 1H), 3.34 (bs, 2H), 3.53 (m, 1H), 4.11 (bs, 1H), 6.69 (bs, 1H), 7.29 (d, J=8 Hz, 2H), 7.63 (d, J=8 Hz, 2H). Anal. (C18 H26 N4 SO6.0.5 EtOAc) C, H, N, S.
  • 9
  • [ 1018332-19-8 ]
  • [ 132622-78-7 ]
  • 10
  • [ 82911-69-1 ]
  • [ 132622-78-7 ]
  • [ 1018332-23-4 ]
 

Historical Records

Technical Information

Categories