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161810

Sigma-Aldrich

5-Chloro-2-methylene-1,3,3-trimethylindoline

technical grade, 95%

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About This Item

Empirical Formula (Hill Notation):
C12H14ClN
CAS Number:
6872-17-9
Molecular Weight:
207.70
EC Number:
229-972-6
MDL number:
MFCD00005814
UNSPSC Code:
12352100
PubChem Substance ID:
24849955
NACRES:
NA.22

grade

technical grade

assay

95%

form

liquid

refractive index

n20/D 1.594 (lit.)

density

1.083 g/mL at 25 °C (lit.)

functional group

chloro

SMILES string

CN1C(=C)C(C)(C)c2cc(Cl)ccc12

InChI

1S/C12H14ClN/c1-8-12(2,3)10-7-9(13)5-6-11(10)14(8)4/h5-7H,1H2,2-4H3

InChI key

VDMXGJJMPKAYQP-UHFFFAOYSA-N

General description

5-Chloro-2-methylene-1,3,3-trimethylindoline undergoes regiospecific 1,3-dipolar cycloaddition reaction with arylnitriloxydes and N-phenylarylnitrilimines.

Application

5-Chloro-2-methylene-1,3,3-trimethylindoline was used in the synthesis of 5′,6-dichloro-1′,3′,3′-trimethyl­spiro­[2H-1-benzopyran-2,2′-indoline].

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
15616HI
08302EI

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Nameer Alhashimy et al.
Acta crystallographica. Section E, Structure reports online, 64(Pt 8), o1430-o1431 (2008-01-01)
In the crystal structure of the title compound, C(19)H(17)Cl(2)NO, the indoline and benzopyran ring systems are approximately perpendicular to each other. The indoline ring is in an envelope conformation with the spiro C atom as the flap. The N atom
Naoual Laghrib et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 2), o374-o374 (2009-01-01)
Two diastereoisomers of the title compound, C(25)H(26)N(2)O, have been prepared by cyclo-addition between 1,3,3-trimethyl-2-methyl-eneindoline and C-phenyl-N-phenyl-nitrone. The stereochemistry of the major diastereoisomer, viz. S,R/R,S, is confirmed by the X-ray analysis. The oxazole and the pyrole rings have envelope conformations. The

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