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1003922-03-9

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  • (S)-2-[3-[(1R,2R)-2-(Dipropylamino)cyclohexyl]thioureido]-N-isopropyl-3,3-dimethylbutanamide

    Cas No: 1003922-03-9

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1003922-03-9 Usage

Description

(S)-2-[3-[(1R,2R)-2-(Dipropylamino)cyclohexyl]thioureido]-N-isopropyl-3,3-dimethylbutanamide is a complex thiourea derivative featuring a cyclohexyl group, two dipropylamino groups, and an N-isopropyl-3,3-dimethylbutanamide group. (S)-2-[3-[(1R,2R)-2-(Dipropylamino)cyclohexyl]thioureido]-N-isopropyl-3,3-dimethylbutanamide is characterized by its unique molecular structure and functional groups, which may contribute to its potential pharmaceutical applications. However, further research is necessary to fully understand its uses and potential benefits.

Uses

Used in Pharmaceutical Industry:
(S)-2-[3-[(1R,2R)-2-(Dipropylamino)cyclohexyl]thioureido]-N-isopropyl-3,3-dimethylbutanamide is used as a potential drug candidate for its unique molecular structure and functional groups, which may offer novel therapeutic opportunities in the treatment of various medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (S)-2-[3-[(1R,2R)-2-(Dipropylamino)cyclohexyl]thioureido]-N-isopropyl-3,3-dimethylbutanamide is used as a subject of study to explore its potential interactions with biological targets and to understand its pharmacological properties. This research may lead to the development of new drugs with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 1003922-03-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,3,9,2 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1003922-03:
(9*1)+(8*0)+(7*0)+(6*3)+(5*9)+(4*2)+(3*2)+(2*0)+(1*3)=89
89 % 10 = 9
So 1003922-03-9 is a valid CAS Registry Number.

1003922-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[[(1R,2R)-2-(dipropylamino)cyclohexyl]carbamothioylamino]-3,3-dimethyl-N-propan-2-ylbutanamide

1.2 Other means of identification

Product number -
Other names (S)-2-(3-((1R,2R)-2-(dipropylamino)cyclohexyl)thioureido)-N-isopropyl-3,3-dimethylbutanamide

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:1003922-03-9 SDS

1003922-03-9Downstream Products

1003922-03-9Relevant articles and documents

Cooperative catalysis by tertiary amino-thioureas: Mechanism and basis for enantioselectivity of ketone cyanosilylation

Zuend, Stephan J.,Jacobsen, Eric N.

, p. 15872 - 15883 (2008/10/09)

The mechanism of the enantioselective cyanosilylation of ketones catalyzed by tertiary amino-thiourea derivatives was investigated using a combination of experimental and theoretical methods. The kinetic analysis is consistent with a cooperative mechanism

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