[A10935] CAS 592-82-5 | 1-Butyl isothiocyanate, 98+% | Alfa
0 ₩
family_key 없음
Brand: Alfa Aesar
592-82-5 | C5H9NS | butyl isothiocyanate
Chemical Identifiers
CAS
592-82-5
Molecular Weight (g/mol)
115.19
Synonym
butyl isothiocyanate
SMILES
CCCCN=C=S
InChI Key
LIMQQADUEULBSO-UHFFFAOYSA-N
Molecular Formula
C5H9NS
IUPAC Name
1-isothiocyanatobutane
Specifications
Appearance (Color)
Clear colorless to pale yellow
Form
Liquid
Assay (GC)
≥98.0%
Refractive Index
1.4985-1.5025 @ 20?C
설명
1-Butyl isothiocyanate participates in the synthesis and characterization of Poly(N-Propargylthiourea). Participates in the Synthesis of 2-Aminobenzothiazoles via Copper (I)-Catalyzed Cross-Coupling with Part-Per-Million Catalyst Loadings. Thiols reactions with 1-Butyl isothiocyanate in aquatic toxicity data in the TETRATOX assay and reactivity data in an abiotic thiol assay. utyl isothiocyanate has been used as capping reagent to immobilize the functionalized derivative of Oregon Green 514 molecular switch on a preformed amino self assembled monlayer.
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
1-Butyl isothiocyanate participates in the synthesis and characterization of Poly(N-Propargylthiourea). Participates in the Synthesis of 2-Aminobenzothiazoles via Copper (I)-Catalyzed Cross-Coupling with Part-Per-Million Catalyst Loadings. Thiols reactions with 1-Butyl isothiocyanate in aquatic toxicity data in the TETRATOX assay and reactivity data in an abiotic thiol assay. utyl isothiocyanate has been used as capping reagent to immobilize the functionalized derivative of Oregon Green 514 molecular switch on a preformed amino self assembled monlayer.
1-Butyl isothiocyanate participates in the synthesis and characterization of Poly(N-Propargylthiourea). Participates in the Synthesis of 2-Aminobenzothiazoles via Copper (I)-Catalyzed Cross-Coupling with Part-Per-Million Catalyst Loadings. Thiols reactions with 1-Butyl isothiocyanate in aquatic toxicity data in the TETRATOX assay and reactivity data in an abiotic thiol assay. utyl isothiocyanate has been used as capping reagent to immobilize the functionalized derivative of Oregon Green 514 molecular switch on a preformed amino self assembled monlayer.
Solubility
Insoluble in water.
Notes
Moisture Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, moisture.
Other References:
UN Number:UN2922Beilstein:906839
GHS Hazard and Precautionary Statements
Hazard Statements:H227-H301+H311+H331-H314
GHS H StatementH331-H314-H318-H227-H302-H312 Toxic if inhaled. Causes severe skin burns and eye damage. Causes serious eye damage. Combustible liquid. Harmful if swallowed. Harmful in contact with skin.
Precautionary Statements:P210-P235-P260-P264b-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P370+P378q-P501c
Risk & Safety
TSCA:YesRTECS Number:NX8420500
경고:RUO – Research Use Only
CAS592-82-5FORMULAC5H9NSHAZARD CLASS6.1EINECS209-770-4MDLMFCD00004824PACKAGING GROUPII
| Pakage | 100g, 25g, 5g |
|---|---|
| brand | Alfa Aesar |
