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Basic information
- CAS
71953-90-7- Standard SMILES
CC(=O)NC(Cc1c[nH]c2ccc(C)cc12)C(=O)O- InChIKey
GTCLKZDZUKYDDV-UHFFFAOYSA-N- Molecular formula
- C14H16N2O3
- Average molar mass
- 260.293 g/mol
- Monoisotopic mass
- 260.11609237
Names & identifiers
- Preferred name
- AG-G-82682
- IUPAC
- N-Acetyl-5-methyltryptophan
- English name
- N-Acetyl-5-methyl-DL-tryptophan
- Molecular formula
- C14H16N2O3
- Molecular weight
- 260.29
Names & synonyms
Ac-Trp(5-Me)-OHAC-5-ME-DL-TRP-OHAC-DL-TRP(5-ME)-OHAC-5-ME-DL-TRYPTOPHANAc-DL-5-MethylTryptophanN-Ac-DL-5-MethylTryptophanACETYL-5-METHYL-DL-TRYPTOPHANTryptophan,N-acetyl-5-methyl-N-Acetyl-5-methyl-DL-tryptophanNα-Acetyl-5-methyl-DL-tryptophan
Database identifiers
- CAS
71953-90-7- PubChem CID
- 3315196
- DTXSID
DTXSID50391379- EC Number
- 118-960-5
Properties
Physicochemical properties
- Melting point
- 165 · 165 - 168oC
- Boiling point
- 587.5 · 587.5±50.0 °C(Predicted)
- Density
- 1.292 · 1.292±0.06 g/cm3(Predicted)
- storage temp.
- 0 °C · Store at 0°C
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 3.56 · 3.56±0.10(Predicted)
- color
- White to Off-White
Chemistry & industry
Applications
UsesN-Acetyl-5-methyl-dl-tryptophan is a useful reagent for the preparation of lactone ketolide macrolide erythromycin antibiotics.
Suppliers13 total
梯希爱（上海）化工贸易有限公司021-61109150 · [email protected]
常州科化生物科技有限公司0519-68985668 13685222090 · [email protected]
上海瀚鸿科技股份有限公司021-54306202 13764082696 · [email protected]
凯试(上海)科技有限公司021-50135380 · [email protected]
吉林中科研伸科技有限公司18143011203 · [email protected]
艾吉析科技（上海）有限公司17721401538;17717235263 17721401538 · [email protected]
淄博百极荣创医药科技有限公司0533-6092686 13371592196 · [email protected]
上海吉尔多肽有限公司+86-21-61263310 13764994101 · [email protected]
滨海吉尔多肽有限公司021-61263389 13524856427 · [email protected]
Nextpeptide Inc+86-0571-81612335 +8613336028439 · [email protected]
DAYANG CHEM (HANGZHOU) CO.,LTD+86-88938639 +86-17705817739 · [email protected]
陕西缔都化学有限公司17691182729 17392216275 · [email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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