| Identification | More | [Name]
5-Chloro-2-methylene-1,3,3-trimethylindoline | [CAS]
6872-17-9 | [Synonyms]
5-CHLORO-1,3,3-TRIMETHYL-2-METHYLENEINDOLINE
5-CHLORO-2,3-DIHYDRO-1,3,3-TRIMETHYL-2-METHYLENE-1H-INDOLE
5-CHLORO-2-METHYLENE-1,3,3-TRIMETHYLINDOLINE
5-chloro-2,3-dihydro-1,3,3-trimethyl-2-methylene-1h-indol
5-CHLORO-2-METHYLENE-1,3,3-TRIMETHYL-IND OLINE, TECH., 95%
1H-Indole, 5-chloro-2,3-dihydro-1,3,3-trimethyl-2-methylene-
1,3,3-Trimethyl-2-methylene-2,3-dihydro-5-chloro-1H-indole
1,3,3-Trimethyl-2-methylene-5-chloro-2,3-dihydro-1H-indole
1,3,3-Trimethyl-2-methylene-5-chloroindoline | [EINECS(EC#)]
229-972-6 | [Molecular Formula]
C12H14ClN | [MDL Number]
MFCD00005814 | [Molecular Weight]
207.7 | [MOL File]
6872-17-9.mol |
| Chemical Properties | Back Directory | [Boiling point ]
139 °C / 11mmHg | [density ]
1.083 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.594(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Inert atmosphere,Room Temperature | [form ]
clear liquid | [pka]
1.12±0.40(Predicted) | [color ]
Orange to Brown to Dark purple | [Specific Gravity]
1.083 | [InChI]
1S/C12H14ClN/c1-8-12(2,3)10-7-9(13)5-6-11(10)14(8)4/h5-7H,1H2,2-4H3 | [InChIKey]
VDMXGJJMPKAYQP-UHFFFAOYSA-N | [SMILES]
CN1C(=C)C(C)(C)c2cc(Cl)ccc12 | [CAS DataBase Reference]
6872-17-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [HS Code ]
29339900 | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Uses]
5-Chloro-2-methylene-1,3,3-trimethylindoline was used in the synthesis of 5′,6-dichloro-1′,3′,3′-trimethyl-spiro-[2H-1-benzopyran-2,2′-indoline]. | [General Description]
5-Chloro-2-methylene-1,3,3-trimethylindoline undergoes regiospecific 1,3-dipolar cycloaddition reaction with arylnitriloxydes and N-phenylarylnitrilimines. |
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