Cas no 177899-21-7 (tert-Butyl N-(tert-Butoxy)carbonyl-N-(4-oxobutyl)carbamate)
Technical Introduction:
tert-Butyl N-(tert-Butoxy)carbonyl-N-(4-oxobutyl)carbamate is a specialized bifunctional protected amine reagent featuring both Boc (tert-butoxycarbonyl) and N-Boc-N-(4-oxobutyl) moieties. Its key advantages include selective reactivity, enabling controlled deprotection and functionalization in multistep syntheses. The 4-oxobutyl group offers a versatile handle for further derivatization, such as reductive amination or nucleophilic additions, while the Boc groups ensure stability under diverse reaction conditions. This compound is particularly useful in peptide chemistry and pharmaceutical intermediates, where orthogonal protection strategies are required. Its high purity and well-defined structure facilitate reproducible results in complex organic transformations.
177899-21-7 structure
Product Name:tert-Butyl N-(tert-Butoxy)carbonyl-N-(4-oxobutyl)carbamate
CAS No:177899-21-7
MF:C14H25NO5
MW:287.352004766464
MDL:MFCD18251622
CID:835604
PubChem ID:10891497
Update Time:2025-06-08
tert-Butyl N-(tert-Butoxy)carbonyl-N-(4-oxobutyl)carbamate Chemical and Physical Properties
Names and Identifiers
-
- Imidodicarbonic acid, 2-(4-oxobutyl)-, 1,3-bis(1,1-dimethylethyl) ester
- di-tert-butyl (4-oxobutyl)imidodicarbonate
- tert-butyl N-[(2-methylpropan-2-yl)oxycarbonyl]-N-(4-oxobutyl)carbamate
- tert-butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate
- Imidodicarbonic acid, (4-oxobutyl)-, bis(1,1-dimethylethyl) ester
- 4-[Bis(tert-butyloxycarbonyl)amino]butanal
- tert-Butyl N-(tert-Butoxy)carbonyl-N-(4-oxobutyl)carbamate
-
- MDL: MFCD18251622
- Inchi: 1S/C14H25NO5/c1-13(2,3)19-11(17)15(9-7-8-10-16)12(18)20-14(4,5)6/h10H,7-9H2,1-6H3
- InChI Key: XTTSZLHDKBNNRZ-UHFFFAOYSA-N
- SMILES: O(C(N(C(=O)OC(C)(C)C)CCCC=O)=O)C(C)(C)C
Computed Properties
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 20
- Rotatable Bond Count: 8
- Complexity: 324
- Topological Polar Surface Area: 72.9
tert-Butyl N-(tert-Butoxy)carbonyl-N-(4-oxobutyl)carbamate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B433095-2.5mg |
tert-Butyl N-[(tert-Butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 2.5mg |
$ 50.00 | 2022-06-07 | ||
| TRC | B433095-5mg |
tert-Butyl N-[(tert-Butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 5mg |
$ 70.00 | 2022-06-07 | ||
| TRC | B433095-25mg |
tert-Butyl N-[(tert-Butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 25mg |
$ 275.00 | 2022-06-07 | ||
| abcr | AB543291-250 mg |
t-Butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate; . |
177899-21-7 | 250MG |
€626.50 | 2022-03-01 | ||
| abcr | AB543291-1 g |
t-Butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate; . |
177899-21-7 | 1g |
€1,192.00 | 2022-03-01 | ||
| Enamine | EN300-303777-0.05g |
tert-butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 95.0% | 0.05g |
$168.0 | 2025-03-19 | |
| Enamine | EN300-303777-0.1g |
tert-butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 95.0% | 0.1g |
$252.0 | 2025-03-19 | |
| Enamine | EN300-303777-0.25g |
tert-butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 95.0% | 0.25g |
$361.0 | 2025-03-19 | |
| Enamine | EN300-303777-0.5g |
tert-butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 95.0% | 0.5g |
$569.0 | 2025-03-19 | |
| Enamine | EN300-303777-1.0g |
tert-butyl N-[(tert-butoxy)carbonyl]-N-(4-oxobutyl)carbamate |
177899-21-7 | 95.0% | 1.0g |
$728.0 | 2025-03-19 |
tert-Butyl N-(tert-Butoxy)carbonyl-N-(4-oxobutyl)carbamate Related Literature
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Shaun D. Wong,Edward I. Solomon Dalton Trans., 2014,43, 17567-17577
-
Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
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4. Estimation of hydrogen sulfide from crude petroleum: a unique invention using a simple chemosensor?Shampa Kundu,Prithidipa Sahoo New J. Chem., 2019,43, 12369-12374
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Saeideh Mirfakhraei,Malak Hekmati,Fereshteh Hosseini Eshbala,Hojat Veisi New J. Chem., 2018,42, 1757-1761
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