2-?????
|
|
2-????? ??
- ???
- -51 °C
- ?? ?
- 228-229 °C (lit.)
- ??
- 1.023 g/mL at 25 °C (lit.)
- ???
- n
20/D 1.569(lit.)
- ???
- 200 °F
- ?? ??
- Keep in dark place,Inert atmosphere,Room temperature
- ???
- ?????, ???? ???
- ?? ?? (pKa)
- 5.26±0.40(Predicted)
- ??? ??
- ??
- Specific Gravity
- 1.02
- ??
- ??? ????? ????
- ?? ??
- -2.4550° (C=1.0 g/100ml, MEOH, 20°C, 589nm)
- ???
- ??? ??
- InChI
- 1S/C9H11N/c1-7-6-8-4-2-3-5-9(8)10-7/h2-5,7,10H,6H2,1H3
- InChIKey
- QRWRJDVVXAXGBT-UHFFFAOYSA-N
- SMILES
- CC1Cc2ccccc2N1
- CAS ??????
- 6872-06-6(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | Xi,Xn | ||
|---|---|---|---|
| ?? ???? ?? | 36/37/38-52/53-22 | ||
| ????? | 26-36/37/39-60-57 | ||
| WGK ?? | 3 | ||
| RTECS ?? | NM1926350 | ||
| ?? ?? ?? | Irritant | ||
| TSCA | TSCA listed | ||
| HS ?? | 29349990 | ||
| ???? ??? | 6.1C - Combustible acute toxic Cat.3 toxic compounds or compounds which causing chronic effects |
||
| Hazard Classifications | Acute Tox. 3 Dermal Acute Tox. 4 Oral Aquatic Acute 1 Eye Irrit. 2 |
2-????? C??? ??, ??, ??
??? ??
CLEAR YELLOW TO BROWN LIQUID??
2-Methylindoline is an intermediate in the production of various indole derivatives?? ??
2-Methylindoline is prepared through the transformation of 1-(2-aminophenyl)propan-2-ol using acidic catalysts[1]. 2-Methylindoline is also produced by the hydrogenation of 2-methylindole in toluene[2].Synthesis Reference(s)
Journal of the American Chemical Society, 111, p. 4108, 1989 DOI: 10.1021/ja00193a056Chemical and Pharmaceutical Bulletin, 26, p. 108, 1978 DOI: 10.1248/cpb.26.108
2-????? ?? ?? ? ???
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?? ??
2-????? ?? ??
???( 318)?? ??
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