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1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,[1S-(1-alpha-,5-alpha-,6-alpha-)]-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113085-29-3

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113085-29-3 Usage

Explanation

This is the full name of the compound, which includes its stereochemistry and the specific atoms or groups that are substituted.

Explanation

This is the mass of one mole of the compound, which is the sum of the atomic weights of all the atoms in the molecular formula.

Explanation

1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,[1S-(1-alpha-,5-alpha-,6-alpha-)]-(9CI) belongs to a specific class of chemical compounds, which are characterized by the presence of a bicyclic structure and an N-methylated amidine group.

Explanation

The compound acts as a selective inhibitor of the enzyme type 2 deiodinase, which is involved in the regulation of thyroid hormone activity.

Explanation

Due to its inhibitory effect on type 2 deiodinase, the compound has been studied for its potential use in treating thyroid disorders and conditions related to thyroid hormone imbalance.
7. Antiviral and Antibacterial Properties

Explanation

The compound has been investigated for its potential antiviral and antibacterial properties, making it a subject of interest in the development of new pharmaceuticals.

Explanation

This part of the name indicates the stereochemistry of the compound, which refers to the three-dimensional arrangement of the atoms in the molecule. The "1S" denotes the configuration at the first carbon atom, while "1-alpha," "5-alpha," and "6-alpha" describe the relative positions of the atoms at the respective carbon positions.

Molecular Weight

238.69 g/mol

Category

N-methylated bicyclic amidine derivatives

Selective Inhibitor

Type 2 deiodinase

Potential Applications

Treatment of thyroid disorders

Stereochemistry

[1S-(1-alpha-,5-alpha-,6-alpha-)]-(9CI)

Check Digit Verification of cas no

The CAS Registry Mumber 113085-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113085-29:
(8*1)+(7*1)+(6*3)+(5*0)+(4*8)+(3*5)+(2*2)+(1*9)=93
93 % 10 = 3
So 113085-29-3 is a valid CAS Registry Number.

113085-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,6-chloro-N-methyl-,[1S-(1-α-,5-α-,6-α-)]-(9CI)

1.2 Other means of identification

Product number -
Other names endo-5-N-Methylcarbomoyl-6-chloro-1,6-diazabicyclo<3.1.0>hexane

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:113085-29-3 SDS

113085-29-3Relevant academic research and scientific papers

1,2-Acyl Migration to an Electron-deficient Nitrogen Atom: a New Rearrangement of Diaziridines without Ring Opening

Denisenko, Sergei N.,Shustov, Gennady V.,Kostyanovsky, Remir G.

, p. 1275 - 1276 (2007/10/02)

5-Acyl-1,6-diazabicyclohexane (1) on treatment with t-butyl hypochlorite affords the corresponding N-chloro-derivative (2) which rearranges easily into 6-acyl-5-chloro-1,6-diazabicyclohexane (3) with a 1,2-shift of the acyl group.

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