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(2S)-(-)-3-exo-(DiMethylaMino)isonorborneol, also known as the dimethylamino derivative of Isoborneol (I780070), is a monoterpene found in various plant essential oils. It is characterized by its dual viricidal activity against herpes simplex virus 1 (HSV-1), making it a promising candidate for pharmaceutical and medical applications.

103729-96-0

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103729-96-0 Usage

Uses

Used in Pharmaceutical Industry:
(2S)-(-)-3-exo-(DiMethylaMino)isonorborneol is used as an antiviral agent for its dual viricidal activity against herpes simplex virus 1 (HSV-1). This property makes it a valuable compound in the development of treatments and preventive measures for HSV-1 infections.
Used in Medical Applications:
In the medical field, (2S)-(-)-3-exo-(DiMethylaMino)isonorborneol is utilized for its potential in combating herpes simplex virus 1 (HSV-1) infections. Its dual viricidal activity offers a promising approach to managing and treating HSV-1-related health issues, providing a new avenue for therapeutic intervention.

Check Digit Verification of cas no

The CAS Registry Mumber 103729-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,2 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103729-96:
(8*1)+(7*0)+(6*3)+(5*7)+(4*2)+(3*9)+(2*9)+(1*6)=120
120 % 10 = 0
So 103729-96-0 is a valid CAS Registry Number.

103729-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Dimethylamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol

1.2 Other means of identification

Product number -
Other names (S)-1,2-dihydroxy-3-butene

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:103729-96-0 SDS

103729-96-0Downstream Products

103729-96-0Relevant academic research and scientific papers

CREATION OF CHIRALITY IN THE REACTION OF THE CHIRAL ESTER ENOLATE-IMINE CONDENSATION LEADING TO THE STEREODIVERGENT SYNTHESIS OF β-LACTAMS

Shimizu, Makoto,Teramoto, Yoshihiro,Fujisawa, Tamotsu

, p. 729 - 732 (1995)

Stereocontrol at C-4 of the β-lactams possessing substituents at 3- and 4-positions in the ester enolate-imine condensation is studied using different metal enolates of the chiral esters possessing amino alcohols derived all from (+)-camphor as an auxiliary, and 4R- or 4S-β-lactam is obtained in a highly stereoselective manner, respectively.The effects of the structure of the chiral auxiliary and the coordination ability of the heteroatoms in the ester part are also dicussed.

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