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(-)-Diisopinocampheyl borane, also known as IpcBH, is a chiral hydroborane reagent derived from the diisopinocampheyl group. It is a versatile and highly selective reducing agent in organic chemistry, known for its ability to transfer hydride ions to various substrates with high enantioselectivity. Its unique structure and properties make it a valuable tool in the synthesis of complex organic molecules and natural products.

21932-54-7

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21932-54-7 Usage

Uses

Used in Organic Synthesis:
(-)-Diisopinocampheyl borane is used as a reducing agent for the asymmetric reduction of prochiral ketones, providing enantiomerically pure secondary alcohols. This application is particularly useful in the synthesis of complex organic molecules and natural products, where stereochemistry plays a crucial role in biological activity and selectivity.
Used in Pharmaceutical Industry:
(-)-Diisopinocampheyl borane is used as a key reagent in the synthesis of enantiomerically pure pharmaceutical compounds. Its ability to selectively reduce prochiral ketones to enantiomerically pure alcohols makes it an invaluable tool in the development of new drugs with improved efficacy and reduced side effects.
Used in Synthesis of Nicotine Analogs:
(-)-Diisopinocampheyl borane is used as a reducing agent in the synthesis of nicotine analogs, which are important compounds for studying the effects of nicotine on the central nervous system and developing new treatments for nicotine addiction and related disorders.
Used in Synthesis of (-)-Invictolide:
(-)-Diisopinocampheyl borane is used as a key reagent in the enantioselective synthesis of (-)-Invictolide, a complex natural product with potential biological activities. Its ability to selectively reduce prochiral ketones to enantiomerically pure alcohols is crucial for obtaining the desired enantiomer of (-)-Invictolide.
Used in Synthesis of (+)-Strictifolione:
(-)-Diisopinocampheyl borane is used as a reducing agent in the enantioselective synthesis of (+)-strictifolione, another complex natural product with potential biological activities. Its high selectivity and ability to transfer hydride ions make it an essential component in the synthesis of (-)-Diisopinocampheyl borane.

Check Digit Verification of cas no

The CAS Registry Mumber 21932-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21932-54:
(7*2)+(6*1)+(5*9)+(4*3)+(3*2)+(2*5)+(1*4)=97
97 % 10 = 7
So 21932-54-7 is a valid CAS Registry Number.

21932-54-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name bis[(1R,3R,4S,5R)-4,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]boron

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21932-54-7 SDS

21932-54-7Upstream product

21932-54-7Relevant academic research and scientific papers

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