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CAS No. : | 628732-03-6 | MDL No. : | MFCD11035916 |
Formula : | C9H9NO | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | GZRHFGSCUQBJHR-UHFFFAOYSA-N |
M.W : | 147.17 | Pubchem ID : | 12119264 |
Synonyms : |
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Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Example SIXTEENbeta Procedure for the synthesis of 7-iodo-indan-1-one (Intermediate SIXTEENbeta3) "2 NHz o'0 v Method J S NaNO2, Kl S /z,, ---- y y Intermediate SIXTEENbeta 1 Intermediate Intermediate SIXTEENbeta3 SIXTEENbeta 2 Use of <strong>[32202-61-2]indan-4-ylamine</strong> (Intermediate SIXTEEN-beta-1) (commercially available from Aldrich) in Method J produced 7-amino-indan-1-one (Intermediate SIXTEENbeta-2). A mixture of [7-AMINO-INDAN-1-ONE] (Intermediate SIXTEENbeta-2) (1.44 g, 9.8 mmol) in water (11 mL), acetic acid (11 mL), and HCl (2.7 [ML)] was treated with a solution [OF NAN02] (0.75 g in 2.8 mL) at [0 C.] A solution of KI in water (1.76 g 10.4 mmol in 2.8 mL) was added and the mixture was heated to [60 C] for 1 h. The mixture was cooled and quenched with solid [NAHS03] followed by water. The product was extracted with CH2Cl2 (3x) and washed with sat. [NAHC03] and brine. The compound was purified by column chromatography on silica gel with 60 to 70% [CH2CL2] : hexane. [7-IODO-INDAN-L-ONE] (Intermediate SIXTEENbeta3) was isolated as a light yellow solid [(31%).] |
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