N-Boc-5-bromoindole can undergo Sonogashira coupling reaction with N,N-diisopropylprop-2-ynylamine to afford the corresponding propargylic diisopropylamine. N-Boc-5-bromoindole is formed as an intermediate during the synthesis of 2-(5-substituted-1H-indol-3-yl)-N-hydroxyacetamide derivatives.
Specifications and Purity: ≥97%
MDL Number: MFCD02090067
Molecular Formula: C13H14BrNO2
Molecular Weight: 296.16
PubChem CID: 2728482
Isomeric SMILES: CC(C)(C)OC(=O)N1C=CC2=C1C=CC(=C2)Br
Related Documents: https://aladdin-for-icloud-store.oss-cn-hangzhou.aliyuncs.com/aladdinsci/pdp/sds/1/I168072-SCI_82ff47c472332d12403e35e6fbdc43bc.pdf
- UPC:
- 51142501
- Condition:
- New
- HazmatClass:
- No
- WeightUOM:
- LB
- MPN:
- I168072-100g
- CAS:
- 182344-70-3
- Product Size:
- 100g
- Hazard Statement Codes:
- H335:H319:H315
- Precautionary Statement Codes:
- P501:P403+P233:P405:P362+P364:P305+P351+P338:P304+P340:P302+P352:P280:P271:P264:P261
akash.verma@cenmed.com
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