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Tetrabutylammonium iodide (C007B-277146)

Catalog No.
C007B-277146
Manufacturer No.
T103714-25g
Manufacturer Name
Aladdin Scientific
Quantity
1
Unit of Measure
EA

Tetrabutylammonium iodide (TBAI) has been used as a catalyst in the following reactions: · Synthesis of O-benzyl-N-Boc-L-tyrosine benzyl ester from N-Boc-L-tyrosine. · Conversion of 8-fluoro-1-aminonaphthalene into

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Tetrabutylammonium iodide (TBAI) has been used as a catalyst in the following reactions: · Synthesis of O-benzyl-N-Boc-L-tyrosine benzyl ester from N-Boc-L-tyrosine. · Conversion of 8-fluoro-1-aminonaphthalene into 1-(8-fluoro-naphthalen-1-yl)piperazine hydrochloride. · Synthesis of 1-(2,4-dichlorophenyl)-5-(4-(4-iodobut-1-ynyl)phenyl)-4-methyl-N-(piperidin-1-yl)-1H-pyrazole-3-carboxamide from 4-(4-(1-(2,4-dichlorophenyl)-4-methyl-3-(piperidin-1-ylcarbamoyl)-1H-pyrazol-5-yl)phenyl)but-3-yn-1-yl methanesulfonate. Other reactions where TBAI can be used as a catalyst: · TBAI-tert-butyl hydroperoxide system can catalyze the conversion of α-methyl styrene derivatives into allylic sulfones by reacting with sulfonylhydrazides under metal-free conditions. · Palladium(0)-catalyzed cross-coupling between benzylic zinc bromides and aryl or alkenyl triflates. · Three-component coupling of amines, carbon dioxide, and halides to form carbamates in the presence of cesium carbonate.

Specifications and Purity: ≥99%

MDL Number: MFCD00011636

Molecular Formula: C16H36NI

Molecular Weight: 369.37

EC Number: 206-220-5

PubChem CID: 67553

Isomeric SMILES: CCCC[N+](CCCC)(CCCC)CCCC.[I-]

Beilstein Registry Number: 3916152

Related Documents: https://aladdin-for-icloud-store.oss-cn-hangzhou.aliyuncs.com/aladdinsci/pdp/sds/1/T103714-SCI_8eefd4800eaef9b95cc29c82ebdda88b.pdf

UPC:
12131507
Condition:
New
HazmatClass:
No
WeightUOM:
LB
MPN:
T103714-25g
CAS:
311-28-4
Product Size:
25g
Hazard Statement Codes:
H335:H319:H315:H302
Precautionary Statement Codes:
P305+P351+P338:P261

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