1,3,3-Trimethyl-2-methyleneindoline
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1,3,3-Trimethyl-2-methyleneindoline
structure -
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CAS No:
118-12-7
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Formula:
C12H15N
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Chemical Name:
1,3,3-Trimethyl-2-methyleneindoline
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Synonyms:
1H-Indole,2,3-dihydro-1,3,3-trimethyl-2-methylene-;Indoline,1,3,3-trimethyl-2-methylene-;2,3-Dihydro-1,3,3-trimethyl-2-methylene-1H-indole;Fischer base;Fischer's base;1,3,3-Trimethyl-2-methyleneindoline;1,3,3-Trimethyl-2-methylene-2,3-dihydroindole;2-Methylene-1,3,3-trimethylindoline;1,2-Dihydro-1,3,3-trimethyl-2-methyleneindole;2,3-Dihydro-1,3,3-trimethyl-2-methyleneindole;1,3-Dihydro-1,3,3-trimethyl-2-methyleneindoline;Fischer's methylene base;NSC 66176;1,3,3-Trimethyl-2-methylene indolenine;1,3,3-Trimethyl-2-methylidene-2,3-dihydro-1H-indole;1,3,3-Trimethyl-2-methylideneindole
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CAS No:
1,3,3-Trimethyl-2-methyleneindoline Basic Attributes
173.25
173.25
131162
204-235-1
66176
DTXSID8051596
29339990
Characteristics
3.2
2.99270
red liquid
0.979 g/mL at 25 °C(lit.)
-8 °C
80 °C @ Press: 0.01 Torr
215 °F
n 20/D 1.577(lit.)
negligible
Store below +30°C.
0.0249mmHg at 25°C
Safety Information
III
9
UN 3082 9/PG 3
2
22-38-50/53
28-60-61-57-37
NM1926500
Xn,N
Stable under normal temperatures and pressures.
P273
H302-H315-H400
|Warning|H302 (97.24%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P273, P280, P301+P312, P302+P352, P321, P330, P332+P313, P362, P391, and P501|Aggregated GHS information provided by 146 companies from 9 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
1,3,3-Trimethyl-2-methyleneindoline Use and Manufacturing
It is prepared by condensation of phenylhydrazine and methyl ethyl ketone, ring-closure reaction, methylation with methyl toluenesulfonate, and neutralization with ammonia. Put water, phenylhydrazine, and sulfuric acid into the reaction pot, heat to 80°C, add methyl ethyl ketone dropwise, and control the feeding temperature at 80-90°C. After the addition, continue to react at 90-100°C for 1.5h. Cool to 70°C, add xylene, let stand to separate the lower layer of water, and wash the xylene layer with water again. Add methyl p-toluenesulfonate, heat, react at 155-160°C for 3 hours, and then react at 160-165°C for 3 hours, dilute the reaction material in water, and add 20% ammonia water dropwise at 70-90°C until the pH is greater than 8. After standing for stratification, the upper oil layer is subjected to vacuum distillation, and the fraction above 80°C (1.33-2.67kPa) is collected as the finished product. The yield is about 70%.
This product can be used as a dye intermediate for the manufacture of cationic golden X-GL, cationic pink FG, cationic brilliant red 5-GN, cationic red 6B, cationic red 3GL, etc.
Intermediates
All other basic organic chemical manufacturing|1H-Indole, 2,3-dihydro-1,3,3-trimethyl-2-methylene-: ACTIVE
Computed Properties
Molecular Weight:173.25
XLogP3:3.4
Hydrogen Bond Acceptor Count:1
Exact Mass:173.120449483
Monoisotopic Mass:173.120449483
Topological Polar Surface Area:3.2
Heavy Atom Count:13
Complexity:229
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Recommended Suppliers of 1,3,3-Trimethyl-2-methyleneindoline
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CN
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1,3,3-Trimethyl-2-methyleneindoline
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