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Merck
모든 사진(2)

주요 문서

348325

Sigma-Aldrich

Boron trichloride solution

1.0 M in heptane

동의어(들):

Boron chloride, Trichloroborane

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About This Item

실험식(Hill 표기법):
BCl3
CAS Number:
Molecular Weight:
117.17
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.22

양식

liquid

Quality Level

반응 적합성

core: boron
reagent type: Lewis acid
reagent type: catalyst

농도

1.0 M in heptane

density

0.74 g/mL at 25 °C

저장 온도

2-8°C

SMILES string

ClB(Cl)Cl

InChI

1S/BCl3/c2-1(3)4

InChI key

FAQYAMRNWDIXMY-UHFFFAOYSA-N

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애플리케이션

  • Boron trichloride, a Lewis acid, is a general reagent for the cleavage of a wide range of ether and acetal protecting groups.
  • It is a useful reagent to directly convert aromatic aldehydes to the corresponding gem-dichlorides.
  • It can also be used in the transmetallation reaction with less nucleophilic reagents such as tin and zirconium organometallic compounds to synthesize a variety of organoboranes.

For preparing methyl esters of fatty acids and for transesterification of triglycerides.

포장

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

법적 정보

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

신호어

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Repr. 1B - Skin Corr. 1B - STOT SE 3

표적 기관

Respiratory system

보충제 위험성

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

35.6 °F - closed cup

Flash Point (°C)

2 °C - closed cup

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

Impact of Different Environmental Stimuli on the Release of 1-MCP from Boron-MCP Complexes.
Shahrin T, et al.
Journal of Plant Studies, 6(1), 46-46 (2016)
Boron Trichloride
Miyaura N, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis (2006)
Migration of 1-alkenyl groups from zirconium to boron compounds.
Cole T E, et al.
Organometallics, 10(10), 3777-3781 (1991)
Conversion of aromatic aldehydes to gem-dichlorides using boron trichloride. A new highly efficient method for preparing dichloroarylmethanes.
Kabalka G W and Wu Z
Tetrahedron Letters, 41(5), 579-581 (2000)
Guillaume Reinisch et al.
The journal of physical chemistry. A, 115(18), 4786-4797 (2011-04-16)
We report on a theoretical study of the gas-phase decomposition of boron trichloride in the presence of hydrogen radicals using ab initio energetic calculations coupled to TST, RRKM, and VTST-VRC kinetic calculations. In particular, we present an addition-elimination mechanism (BCl(3)

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