Cas no 18209-14-8 (N-Methyl Mitomycin A)
N-Methyl Mitomycin A structure
Product Name:N-Methyl Mitomycin A
CAS No:18209-14-8
MF:C17H21N3O6
MW:363.365144491196
CID:202296
PubChem ID:159845
Update Time:2025-04-19
N-Methyl Mitomycin A Chemical and Physical Properties
Names and Identifiers
-
- Azirino[2',3':3,4]pyrrolo[1,2-a]indole-4,7-dione,8-[[(aminocarbonyl)oxy]methyl]-1,1a,2,8,8a,8b-hexahydro-6,8a-dimethoxy-1,5-dimethyl-,(1aS,8S,8aR,8bS)-
- 6-O-Methyl Mycophenolic Acid Methyl Ester-d9
- Azirino[2',3':3,4]pyrrolo[1,2-a]indole-4,7-dione,8-[[(aminocarbonyl)oxy]methyl]-1,1a,2,8,8a,8b-hexahydro-6,8a-dimethoxy-1,5-d
- Mitomycin F
- N-Methyl Mitomycin A
- 004820
- 1-Methyl-3-chlormethyl-pyrrolidin
- 3-Chlormethyl-1-methyl-pyrrolidin
- 3-chloromethyl-1-methylpyrrolidine
- 3-chloromethyl-1-methyl-pyrrolidine
- AC1NP9CZ
- CTK5A8702
- N-metil-3-clorometilpirrolidina
- N-metylmitomycin A
- SBB012983
- SureCN28718
- ZERO
- UNII-GOQ83S599K
- 18209-14-8
- AZIRINO(2',3':3,4)PYRROLO(1,2-A)INDOLE-4,7-DIONE, 8-(((AMINOCARBONYL)OXY)METHYL)-1,1A,2,8,8A,8B-HEXAHYDRO-6,8A-DIMETHOXY-1,5-DIMETHYL-, (1AS,8S,8AR,8BS)-
- FMMDHGNWABITNT-JZWICRQDSA-N
- Q27279211
- Azirino(2',3':3,4)pyrrolo(1,2-a)indole-4,7-dione, 8-(((aminocarbonyl)oxy)methyl)-1,1a,2,8,8a,8b-hexahydro-6,8a-dimethoxy-1,5-dimethyl-, (1aS-(1aalpha,8beta,8aalpha,8balpha))-
- N-Methylmitomycin A
- Azirino(2',3':3,4)pyrrolo(1,2-a)indole-4,7-dione, 1,1a,2,8,8a,8b-hexahydro-6,8a-alpha-dimethoxy-1,5-dimethyl-8-(hydroxymethyl)-, carbamate (ester)
- (6,8a-Dimethoxy-1,5-dimethyl-4,7-dioxo-1,1a,2,4,7,8,8a,8b-octahydroazireno[2',3':3,4]pyrrolo[1,2-a]indol-8-yl)methyl hydrogen carbonimidate
- GOQ83S599K
- Azirino[2',3':3,4]pyrrolo[1,2-a]indole-4,7-dione, 8-[[(aminocarbonyl)oxy]methyl]-1,1a,2,8,8a,8b-hexahydro-6,8a-dimethoxy-1,5-dimethyl-, (1aS,8S,8aR,8bS)-
- CHEMBL102817
- [(4S,6S,7R,8S)-7,11-dimethoxy-5,12-dimethyl-10,13-dioxo-2,5-diazatetracyclo[7.4.0.02,7.04,6]trideca-1(9),11-dien-8-yl]methyl carbamate
- AKOS030241636
- DTXSID40939522
- N-METHYL-MITOMYCIN A
-
- Inchi: 1S/C17H21N3O6/c1-7-12(21)11-10(13(22)14(7)24-3)8(6-26-16(18)23)17(25-4)15-9(19(15)2)5-20(11)17/h8-9,15H,5-6H2,1-4H3,(H2,18,23)/t8-,9+,15+,17-,19?/m1/s1
- InChI Key: FMMDHGNWABITNT-JZWICRQDSA-N
- SMILES: O(C)[C@@]12[C@H](COC(N)=O)C3C(C(=C(C)C(C=3N1C[C@H]1[C@@H]2N1C)=O)OC)=O
Computed Properties
- Exact Mass: 363.143
- Monoisotopic Mass: 363.143
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 8
- Heavy Atom Count: 26
- Rotatable Bond Count: 5
- Complexity: 802
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 4
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 0.3
- Topological Polar Surface Area: 111A^2
Experimental Properties
- Density: 1.46
- Boiling Point: 568°Cat760mmHg
- Flash Point: 297.3°C
- Refractive Index: 1.633
N-Methyl Mitomycin A Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | M323080-2.5mg |
N-Methyl Mitomycin A |
18209-14-8 | 2.5mg |
$ 224.00 | 2023-09-07 | ||
| TRC | M323080-25mg |
N-Methyl Mitomycin A |
18209-14-8 | 25mg |
$ 1694.00 | 2023-09-07 | ||
| Biosynth | TAA20914-1 mg |
N-Methyl mitomycin A |
18209-14-8 | 1mg |
$167.48 | 2023-01-02 | ||
| Biosynth | TAA20914-5 mg |
N-Methyl mitomycin A |
18209-14-8 | 5mg |
$544.35 | 2023-01-02 | ||
| Biosynth | TAA20914-10 mg |
N-Methyl mitomycin A |
18209-14-8 | 10mg |
$870.90 | 2023-01-02 | ||
| Biosynth | TAA20914-25 mg |
N-Methyl mitomycin A |
18209-14-8 | 25mg |
$1,633.00 | 2023-01-02 | ||
| Biosynth | TAA20914-50 mg |
N-Methyl mitomycin A |
18209-14-8 | 50mg |
$2,613.00 | 2023-01-02 |
N-Methyl Mitomycin A Related Literature
-
1. Structurally modified antitumour agents. Part 1. Synthesis of cyclopropapyrrolo[1,2-a]indoles related to mitosenes by intramolecular cycloadditionGraham B. Jones,Christopher J. Moody J. Chem. Soc. Perkin Trans. 1 1989 2449
Related Categories
- Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Indolequinones Mitomycins, mitosane and mitosene derivatives
- Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Mitomycins, mitosane and mitosene derivatives
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