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(2S,3R)-3-[(dimethylamino)methyl]bicyclo[2.2.1]hept-5-en-2-ylmethanol, also known as dicyclohexylcarbodiimide, is a chemical compound with a bicyclic structure featuring a hydroxyl group and a dimethylamino functional group. This versatile reagent is widely utilized in organic and medicinal chemistry for the synthesis of peptide bonds and other amide-containing compounds, making it a valuable building block for creating complex organic molecules.

56679-25-5

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56679-25-5 Usage

Uses

Used in Pharmaceutical Industry:
(2S,3R)-3-[(dimethylamino)methyl]bicyclo[2.2.1]hept-5-en-2-ylmethanol is used as a peptide coupling reagent for the synthesis of pharmaceuticals. It activates carboxylic acids to form amide bonds with amines, which is crucial in the production of various biologically active compounds.
Used in Agrochemical Industry:
In the agrochemical industry, (2S,3R)-3-[(dimethylamino)methyl]bicyclo[2.2.1]hept-5-en-2-ylmethanol is employed as a reagent for the synthesis of agrochemicals. Its ability to facilitate the formation of amide bonds is essential in creating compounds that can be used in the development of pesticides and other agricultural products.
Used in Organic Chemistry:
(2S,3R)-3-[(dimethylamino)methyl]bicyclo[2.2.1]hept-5-en-2-ylmethanol is used as a building block in organic chemistry for the synthesis of complex organic molecules. Its unique bicyclic structure and functional groups make it a valuable component in the creation of a wide range of compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 56679-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,7 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56679-25:
(7*5)+(6*6)+(5*6)+(4*7)+(3*9)+(2*2)+(1*5)=165
165 % 10 = 5
So 56679-25-5 is a valid CAS Registry Number.

56679-25-5SDS

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 [2-[(dimethylamino)methyl]-3-bicyclo[2.2.1]hept-5-enyl]methanol

1.2 Other means of identification

Product number -
Other names endo-cis-2,3-Dicarboxy-bicyclo[2.2.1]hept-5-en-spiro[7]cyclopropan[1']-anhydrid

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:56679-25-5 SDS

56679-25-5Relevant academic research and scientific papers

Synthesis of the D2d-Dinoradamantane Derivatives Having Two Coaxially Oriented Unsaturated Centers. 6-Methylene-D2d-dinoradamantan-2-one and D2d-Dinoradamantane-2,6-dione

Nakazaki, Masao,Naemura, Koichiro,Harada, Hiroshi,Narutaki, Hideya

, p. 3470 - 3474 (2007/10/02)

From the cyclopentadiene-maleic anhydride adduct was prepared the norbornenecarboxylic acid 22.Treatment of the acid chloride 23 with triethylamine afforded the tetracyclic ketone 24 which was converted into the dinoradamantanecarboxylic acid 25 by a basic ring-opening reaction.The sequence of conversions involving the Cope elimination of the amine oxide derived from the amine 31 provided 6-methylene-D2d-dinoradamantan-2-one (6) whose OsO4-NaIO4 oxidation eventually yielded D2d-dinoradamantane-2,6-dione (7) of D2 symmetry.

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