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(+)-DIP-BROMIDE(TM) is a chiral catalyst that plays a crucial role in various organic synthesis processes. It is particularly effective in facilitating asymmetric reactions, which are essential for the production of enantiomerically pure compounds. These compounds are vital in the pharmaceutical industry, as they can exhibit different biological activities and properties.

112246-74-9

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112246-74-9 Usage

Uses

Used in Pharmaceutical Industry:
(+)-DIP-BROMIDE(TM) is used as a chiral catalyst for asymmetric DIels-Alder reactions. This application is significant because it allows for the selective synthesis of specific enantiomers, which are crucial in the development of drugs with desired biological activities and reduced side effects.
Used in Organic Synthesis:
(+)-DIP-BROMIDE(TM) is also used as a catalyst in the Pictet-Spengler reaction, a type of organic reaction that involves the cyclization of a primary amine with an aldehyde or ketone to form a tetrahydroisoquinoline. This reaction is important in the synthesis of various natural products and pharmaceutical compounds, making (+)-DIP-BROMIDE(TM) a valuable tool in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 112246-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,4 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112246-74:
(8*1)+(7*1)+(6*2)+(5*2)+(4*4)+(3*6)+(2*7)+(1*4)=89
89 % 10 = 9
So 112246-74-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H34BBr/c1-11-15-7-13(19(15,3)4)9-17(11)21(22)18-10-14-8-16(12(18)2)20(14,5)6/h11-18H,7-10H2,1-6H3/t11-,12-,13?,14?,15?,16?,17-,18-/m0/s1

112246-74-9 Well-known Company Product Price

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  • Aldrich

  • (414271)  (+)-DIP-Bromide  95%

  • 112246-74-9

  • 414271-5G

  • 1,487.07CNY

  • Detail

112246-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names (1S)-(+)-B-Bromodiisopinocampheylborane

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:112246-74-9 SDS

112246-74-9Relevant academic research and scientific papers

Enantioselective Ring Cleavage of meso-Epoxides with B-Halodiisopinocampheylboranes

Joshi, N. N.,Srebnik, M.,Brown, Herbert C.

, p. 6246 - 6248 (2007/10/02)

Asymmetric synthesis starting from meso compounds is an increasingly important method for the preparation of optically active compound.We now report the synthesis of optically active 1,2-halohydrins using B-halodiisopinocampheylboranes, Ipc2BX (1a-c).

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