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CHEMDOR CHEMICALS CATALOG

1H-Indazole-5-boronic acid

1H-Indazole-5-boronic acid • CHA.75321 • CAS 338454-14-1

≥95%

Catalogued Pack Sizes Technical Data Safety Context B2B Inquiry Ready
1H-Indazole-5-boronic acid molecular structure
Ordering
Available Variants
2 Variants
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250 mg
SKU
CHA.75321-250mg
Price
€107.20
Available – Dispatch in 14 days
1 g
SKU
CHA.75321-1g
Price
€171.00
Available – Dispatch in 14 days
Availability & Stock Pack SKU Price (EUR)
Available – Dispatch in 14 days
Global Network - International delivery
250 mg CHA.75321-250mg €107.20
Available – Dispatch in 14 days
Global Network - International delivery
1 g CHA.75321-1g €171.00
Product Overview

≥95%

SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Quick Product Snapshot
Product Type Research Chemical / Reference Material
CAS Number 338454-14-1
Packaging Multiple pack-size options available
Fulfillment International B2B Freight (Dubai Hub)
Technical Specifications Structured product data
Empirical Formula (Hill Notation) C7H7BN2O2
CAS Number 338454-14-1
Molecular Weight 161.95
NACRES NA.22
PubChem Substance ID 329764051
UNSPSC Code 12352103
MDL number MFCD06739151
Safety Information Handling visibility
pictograms
GHS07
GHS07 pictogram
GHS07
signalword Warning
hcodes H302
Hazard Classifications Acute Tox. 4 Oral
Storage Class 11 - Combustible Solids
wgk WGK 1
flash_point_f Not applicable
flash_point_c Not applicable
Technical Overview & Applications Use-case context
1H-Indazole-5-boronic acid, with the CAS registry number 338454-14-1, is a boronic acid derivative of indazole, a fused heterocyclic compound. This compound has been utilized as a building block in various organic synthesis reactions, particularly in the formation of complex molecules through cross-coupling reactions. The presence of the boronic acid functional group allows for the participation in Suzuki-Miyaura coupling reactions, facilitating the creation of carbon-carbon bonds with aryl halides. As a result, 1H-Indazole-5-boronic acid has found applications in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its unique chemical properties make it a valuable intermediate in the synthesis of a wide range of compounds, and its reactivity has been explored in various chemical transformations, showcasing its potential as a versatile synthetic tool.

Supply Chain & Fulfillment Operations

Chemdor Chemicals L.L.C., Dubai, United Arab Emirates supports structured B2B procurement workflows for 1H-Indazole-5-boronic acid (CAS 338454-14-1) .

  • Supplier-managed sourcing and fulfillment workflows
  • Research-scale and bulk supply via international freight networks
  • Batch-level documentation support for technical compliance and procurement review

Supporting laboratory, research, and industrial procurement operations across international markets.

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