34404-30-3
34404-30-3 structure
- Name: Boc-D-glutamic acid α-benzylester
- Chemical Name: Boc-D-Glu-OBzl
- CAS Number: 34404-30-3
- Molecular Formula: C17H23NO6
- Molecular Weight: 337.368
- Catalog: Biochemical Amino acids and their derivatives Glutamic acid derivative
- Create Date: 2019-01-09 11:52:01
- Modify Date: 2026-07-01 12:43:48
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Boc-D-Glu-OBzl is a glutamic acid derivative[1].
| Name | Boc-D-Glu-OBzl |
|---|---|
| Synonyms |
(4R)-5-(Benzyloxy)-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid
N-ALPHA-TERT-BUTYLOXYCBONYL-D-GLUTAMIC ACID GAMMA-BENZYL ESTER N-Boc-D-glutaMic acid 1-benzyl ester BOC-D-GLUTAMIC ACID-ALPHA-BENZYL ESTER BOC-D-GLUTAMIC ACID GAMMA-BENZYL ESTER Boc-D-glutamic acid 5-tert-butyl ester Boc-D-GL 1-Benzyl N-Boc-D-glutamate (4R)-5-(benzyloxy)-4-{[(tert-butoxy)carbonyl]amino}-5-oxopentanoic acid Boc-D-Glu-OtBu (R)-5-(benzyloxy)-2-((tert-butoxycbonyl)amino)-5-oxopentanoic acid N-ALPHA-T-BUTOXYCBONYL-D-GLUTAMIC ACID GAMMA-BENZYL ESTER N-T-BUTOXYCBONYL-D-GLUTAMIC ACID-ALPHA-BENZYL ESTER (4R)-5-(Benzyloxy)-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) Boc-D-Glu-OBn Boc-D-g Boc-D-Glu-OBzl //BP (4R)-4-[(2-methylpropan-2-yl)oxycbonylamino]-5-oxo-5-phenylmethoxypentanoic acid BOC-D-GLU-OBZL (34-3) BOC-D-GLU-OBZL Boc-D-glutamic acid α-benzyl ester N-TERT-BUTOXYCBONYL-D-GLUTAMIC ACID ALPHA-BENZYL ESTER N-tert-Butoxycbonyl-D-glutamic acid α-benzyl ester Boc-D-glutamic acid-α-benzyl ester D-Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl) ester N-ALPHA-T-BOC-D-GLUTAMIC ACID GAMMA-BENZYL ESTER Boc-D-glutaMic acid-beta-benzyl ester 1-Benzyl N-(tert-Butoxycbonyl)-D-glutamate N-(tert-Butoxycarbonyl)-D-glutamic Acid 1-Benzyl Ester 1-BenzylN-(tert-Butoxycbonyl)-D-glutamate> T-BUTYLOXYCBONYL-D-GLUTAMIC ACID GAMMA-BENZYL ESTER BOC-D-GLU(BZL)-OH BOC-D-GLUTAMIC ACID 1-BENZYL ESTER TIANFUCHEM-34-3-High purity Boc-D-Glu-OBzl factory price N-t-Boc-D-glutamicacid1-benzylester D-Glutamic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(phenylmethyl)ester 1-Benzyl N-(tert-Butoxycarbonyl)-D-glutamate BOC-D-GLUTAMIC ACID-A-BENZYLESTER Boc-D-Glu-OBz BOC-D-GLUTAMIC ACID-OBZL (Tert-Butoxy)carbonyl D-Glu-OBzl N-Boc-D-Glutamic Acid 1-Benzyl Ester (4S)-5-(Benzyloxy)-4-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) N-ALPHA-T-BOC-D-GLUTAMIC ACID ALPHA-BENZYL ESTER Boc-D-Glu(OBzl)-OH N-tert-Butoxycbonyl-D-glutamic acid 2-benzyl Boc- D -Glu-OBzl MFCD00038266 N-Boc-D-glutamic Acid Benzyl Ester (R)-5-(Benzyloxy)-4-((tert-butoxycbonyl)amino)-5-oxopentanoicacid N-alpha-t-Butyloxycbonyl-D-glutamic acid benzyl ester (4S)-5-(Benzyloxy)-4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)-5-oxopentanoic acid N-tert-Butoxycbonyl-D-glutamic acid 1-benzyl ester N-T-BOC-D-GLUTAMIC ACID A-BENZYL ESTER Boc-D-glutamic acid 1-benzyl ester BOC-D-GLUTAMIC ACID-Y-BENZYLESTER BOC-D-GLU(OBZL)-OH BOC-D-GLUTAMIC ACID(OBZL)-OH |
| Description | Boc-D-Glu-OBzl is a glutamic acid derivative[1]. |
|---|---|
| Related Catalog | |
| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 522.6±50.0 °C at 760 mmHg |
| Melting Point | 98 °C |
| Molecular Formula | C17H23NO6 |
| Molecular Weight | 337.368 |
| Flash Point | 269.9±30.1 °C |
| Exact Mass | 337.152527 |
| PSA | 101.93000 |
| LogP | 3.43 |
| Vapour Pressure | 0.0±1.4 mmHg at 25°C |
| Index of Refraction | 1.524 |
| Storage condition | 0-6°C |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | T+ |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2924299090 |
|
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34404-30-3 |
| Literature: Roczniki Chemii, , vol. 48, p. 1921 - 1927 |
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34404-30-3 |
| Literature: Roczniki Chemii, , vol. 48, p. 1921 - 1927 |
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34404-30-3 |
| Literature: Roczniki Chemii, , vol. 48, p. 1921 - 1927 |
| Precursor 4 | |
|---|---|
| DownStream 8 | |
![[(3R,6S)-6-(2,3-difluorophenyl)-2-oxoazepan-3-yl]carbamate structure](https://image.chemsrc.com/caspic/352/781650-32-6.png)
![1-Benzyl 5-methyl N,N-bis{[(2-methyl-2-propanyl)oxy]carbonyl}-D-g lutamate structure](https://image.chemsrc.com/caspic/083/784156-32-7.png)
![Benzyl (2R,5E)-2-(bis{[(2-methyl-2-propanyl)oxy]carbonyl}amino)-6 -nitro-5-hexenoate structure](https://image.chemsrc.com/caspic/045/784156-33-8.png)
![Benzyl N,N-bis{[(2-methyl-2-propanyl)oxy]carbonyl}-5-oxo-D-norval inate structure](https://image.chemsrc.com/caspic/007/784156-34-9.png)
![(5S)-5-(2,3-Difluorophenyl)-N2,N2-bis{[(2-methyl-2-propanyl)oxy]carbonyl}-D-lysine structure](https://image.chemsrc.com/caspic/169/784156-96-3.png)
![Benzyl (5S)-5-(2,3-difluorophenyl)-N,N-bis{[(2-methyl-2-propanyl) oxy]carbonyl}-6-nitro-D-norleucinate structure](https://image.chemsrc.com/caspic/470/880144-45-6.png)
![1-Benzyl 5-methyl N-{[(2-methyl-2-propanyl)oxy]carbonyl}-D-glutam ate structure](https://image.chemsrc.com/caspic/045/883985-06-6.png)
| HS Code | 2924299090 |
|---|---|
| Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |