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Triethylborane

Catalog No. 257192 Name Sigma Aldrich
CAS Number 97-94-9 Website http://www.sigmaaldrich.com
M. F. C6H15B Telephone 1-800-521-8956
M. W. 97.9943 Fax
Purity ≥95% Email
Storage Chembase ID: 129989

SYNONYMS

Title
三乙基硼
IUPAC name
triethylborane
IUPAC Traditional name
triethylborane
Synonyms
triethylboron

DATABASE IDS

EC Number 202-620-9
MDL Number MFCD00009022
PubChem SID 24855572
CAS Number 97-94-9

PROPERTIES

Personal Protective Equipment Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P222-P231-P280-P301 + P310-P305 + P351 + P338-P422
RID/ADR UN 2845 4.2/PG 1
Risk Statements 17-22-34
RTECS ED2100000
Safety Statements 7-23-26-36/37/39-43-45
Hazard Class 4.2
UN Number 2845
Packing Group 1
German water hazard class 3
GHS Pictograms GHS02
GHS Pictograms GHS05
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H250-H301-H314
European Hazard Symbols Flammable Flammable (F)
European Hazard Symbols Corrosive Corrosive (C)
MSDS Link Download
Linear Formula (C2H5)3B
Purity ≥95%
Boiling Point 95 °C(lit.)
Density 0.677 g/mL at 25 °C(lit.)
Flash Point -36 °C
Flash Point -32.8 °F
Melting Point -93 °C(lit.)
Refractive Index n20/D 1.397(lit.)

DETAILS

Description (English)
Packaging
100 g in Sure-Pac™
Application
Reagent for:
• Enantioselective umpolung allylation of aldehydes1
• Preparation of tetramethylammonium trialkylphenylborate salts2Catalyst for:
• Radical reductions of alkyl bromides and iodides bearing electron withdrawing groups with N-heterocyclic carbene boranes3
• Synthesis of 1-substituted pyrrolines by N-diallylation of amines and ring-closing metathesis4
• Decarboxylative C-C bond cleavage reactions5
• Alkene hydrogenations6
• Aminyl radical cyclizations onto silyl enol ethers7Modifier for single-site organochromium ethylene polymerization catalysts8
Used with lithium tri-tert-butoxyaluminohydride (cat. no. L2904) in the reductive cleavage of ethers and epoxides. Used in the deoxygenation of primary and secondary alcohols.
Recommended products
Angled septum-inlet adapter Z118206 or straight septum-inlet adapter, 6mm I.D. inlet, Z118141 or straight septum-inlet adapter, 13mm I.D. inlet, Z118192 is recommended.
Description (简体中文)
包装
100 g in Sure-Pac™
Application
Reagent for:
• Enantioselective umpolung allylation of aldehydes1
• Preparation of tetramethylammonium trialkylphenylborate salts2Catalyst for:
• Radical reductions of alkyl bromides and iodides bearing electron withdrawing groups with N-heterocyclic carbene boranes3
• Synthesis of 1-substituted pyrrolines by N-diallylation of amines and ring-closing metathesis4
• Decarboxylative C-C bond cleavage reactions5
• Alkene hydrogenations6
• Aminyl radical cyclizations onto silyl enol ethers7Modifier for single-site organochromium ethylene polymerization catalysts8
与三叔丁氧基氢化铝锂(产品目录号 L2904)共同用于醚和环氧化物的还原裂解反应。可用于伯醇和仲醇的脱氧反应。
Recommended products
建议使用弯通式隔垫入口接头 Z118206 或直通式隔垫入口接头 Z118141(6mm 内径入口)或直通式隔垫入口接头 Z118192(13mm 内径入口)。

REFERENCES