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1-[[(1Z)-1-[(N,N-dimethylcarbamimidoyl)hydrazinylidene]propan-2-ylidene]amino]-2,3-dimethyl-guanidine is a complex organic compound with the molecular formula C9H20N6. It is characterized by a guanidine core, which is a common structural motif in various biologically active molecules. The compound features a 1-amino-2,3-dimethylguanidine moiety, which is a derivative of guanidine with two methyl groups attached to the second and third carbon atoms. The unique aspect of 1-[[(1Z)-1-[(N,N-dimethylcarbamimidoyl)hydrazinylidene]propan-2-ylidene]amino]-2,3-dimethyl-guanidine is the presence of a (1Z)-1-[(N,N-dimethylcarbamimidoyl)hydrazinylidene]propan-2-ylidene group, which adds to the molecule's complexity and potential reactivity. This group includes a hydrazino moiety connected to a dimethylcarbamimidoyl group, indicating the presence of a urea-like structure with two methyl groups attached to the nitrogen. The Z configuration suggests that the double bond in the propane-2-ylidene part of the molecule has a specific geometric arrangement. 1-[[(1Z)-1-[(N,N-dimethylcarbamimidoyl)hydrazinylidene]propan-2-ylidene]amino]-2,3-dimethyl-guanidine may have potential applications in pharmaceuticals or as a chemical intermediate due to its intricate structure and functional groups.

7069-33-2

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7069-33-2 Usage

Contains a guanidine group

A functional group with a carbon atom double bonded to a nitrogen atom and single bonded to two other nitrogen atoms.

Contains a dimethylcarbamimidoyl hydrazine group

A functional group with a carbonyl group (C=O) bonded to a nitrogen atom, which is further bonded to two methyl groups and a hydrazine group (NH-NH2).

Highly reactive

Due to the presence of multiple nitrogen atoms and the nature of the functional groups, the compound can readily participate in chemical reactions.

Potentially toxic

The presence of the guanidine and dimethylcarbamimidoyl hydrazine groups may contribute to the compound's toxicity.

Applications in pharmaceuticals

The compound's reactivity and unique structure may make it useful in the development of new drugs or drug candidates.

Use as a reagent in organic synthesis

The compound's reactivity can be harnessed to facilitate specific chemical reactions in the synthesis of other organic compounds.

Research tool in biochemistry

The compound's unique structure and reactivity may be useful in studying biological processes or as a probe to investigate specific biochemical interactions.

Controlled laboratory setting

Due to its potential hazards, the compound should be handled and used in a controlled environment with proper safety measures in place.

Knowledgeable and trained personnel

Only those with the appropriate expertise and training should work with this complex and potentially hazardous compound.

Check Digit Verification of cas no

The CAS Registry Mumber 7069-33-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7069-33:
(6*7)+(5*0)+(4*6)+(3*9)+(2*3)+(1*3)=102
102 % 10 = 2
So 7069-33-2 is a valid CAS Registry Number.

7069-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(Z)-[(1E)-1-[(N,N'-dimethylcarbamimidoyl)hydrazinylidene]propan-2-ylidene]amino]-2,3-dimethylguanidine,hydroiodide

1.2 Other means of identification

Product number -
Other names -

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:7069-33-2 SDS

7069-33-2Upstream product

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