[A14839] CAS 4659-45-4 | 2,6-Dichlorobenzoyl chloride, 98% | Alfa
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Brand: Alfa Aesar
4659-45-4 | C7H3Cl3O | 2,6-dichlorobenzoyl chloride
Chemical Identifiers
CAS
4659-45-4
Molecular Weight (g/mol)
209.45
Synonym
2,6-dichlorobenzoyl chloride
SMILES
ClC(=O)C1=C(Cl)C=CC=C1Cl
InChI Key
JBLIDPPHFGWTKU-UHFFFAOYSA-N
Molecular Formula
C7H3Cl3O
IUPAC Name
2,6-dichlorobenzoyl chloride
Specifications
Refractive Index
1.5580-1.5620 @ 20?C
Assay (GC)
≥97.5%
Appearance (Color)
Clear colorless to pale yellow
Form
Liquid
설명
2,6-Dichlorobenzoyl chloride acts as an important intermediate in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. It is employed in the substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases. It is also used in the preparation of 1-acyliridoles and (-)-aspicilin. In addition to this, it undergoes esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,6-Dichlorobenzoyl chloride acts as an important intermediate in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. It is employed in the substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases. It is also used in the preparation of 1-acyliridoles and (-)-aspicilin. In addition to this, it undergoes esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.
2,6-Dichlorobenzoyl chloride acts as an important intermediate in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs. It is employed in the substrate activity screening method for the rapid development of novel substrates and their conversion into non-peptidic inhibitors of Cys and Ser proteases. It is also used in the preparation of 1-acyliridoles and (-)-aspicilin. In addition to this, it undergoes esterification of (fluoren-9-ylmethoxy)carbonyl (Fmoc)-amino acids to 4-alkoxybenzyl alcohol polystyrene.
Solubility
Miscible with alcohol, ether and acetone. Slightly miscible with heptane. Immiscible with water.
Notes
Moisture sensitive. Incompatible with alcohols, oxidizing agents and strong bases.
Other References:
UN Number:UN3265Beilstein:639531
GHS Hazard and Precautionary Statements
Hazard Statements:H314
GHS H StatementH314-H318Causes severe skin burns and eye damage.Causes serious eye damage.
Precautionary Statements:P260-P264b-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c
Risk & Safety
TSCA:No
경고:RUO – Research Use Only
CAS4659-45-4FORMULAC7H3Cl3OHAZARD CLASS8EINECS225-102-4MDLMFCD00000662PACKAGING GROUPII
| Pakage | 10g, 50G |
|---|---|
| brand | Alfa Aesar |
