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1-(Cyclohexyl-(phenylthiocarbamoyl)phosphanyl)-N-phenyl-methanethioamide is a complex organic compound with the molecular formula C20H23N2PS2. It is a derivative of thiocarbamate, featuring a cyclohexyl group, a phenylthiocarbamoyl group, a phosphanyl group, and an N-phenyl-methanethioamide group. 1-(cyclohexyl-(phenylthiocarbamoyl)phosphanyl)-N-phenyl-methanethioamide is characterized by its unique structure, which includes a cyclohexane ring, a phenyl ring, and two sulfur atoms bonded to the phosphorus atom. It is likely to have applications in the fields of agrochemicals, pharmaceuticals, or as a precursor in the synthesis of other complex molecules. Due to its specific functional groups and structural features, it may exhibit unique chemical properties and reactivity, making it a potential candidate for further research and development in various chemical and biological contexts.

977-69-5

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977-69-5 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Phosphorus-containing compound

Explanation

The compound contains a phosphorus atom, which is a key component of its structure and reactivity.
3. Thiocarbamoyl group

Explanation

A functional group consisting of a carbon, sulfur, and nitrogen atoms, which is attached to the phosphorus atom in the compound.
4. Phenyl group

Explanation

An aromatic ring consisting of six carbon atoms with alternating single and double bonds, which is also attached to the phosphorus atom.
5. Chemical processes and reactions

Explanation

The compound is used as a reagent or catalyst in various chemical processes and reactions, indicating its versatility and potential applications.
6. Biological activity

Explanation

The compound is known to exhibit biological activity, suggesting that it may have potential applications in pharmaceuticals or other fields.
7. Further research needed

Explanation

More research is required to fully understand the compound's potential applications and its effects on biological systems.
8. Complex structure

Explanation

The compound's intricate arrangement of atoms and functional groups makes it an interesting subject for further study and exploration in the field of chemistry.
9. Potential applications

Explanation

The compound's unique properties and reactivity may lead to its use in various industries, such as pharmaceuticals, materials science, or chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 977-69-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 977-69:
(5*9)+(4*7)+(3*7)+(2*6)+(1*9)=115
115 % 10 = 5
So 977-69-5 is a valid CAS Registry Number.

977-69-5SDS

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 1-[cyclohexyl(phenylcarbamothioyl)phosphanyl]-N-phenylmethanethioamide

1.2 Other means of identification

Product number -
Other names Cyclohexyl-bis-<N-phenyl-thiocarbamoyl>-phosphin

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:977-69-5 SDS

977-69-5Downstream Products

977-69-5Relevant academic research and scientific papers

The reactions of hetero-allenes RN=C=X with phosphine derivatives containing a P-H bond

Thewissen, D. H. M. W.,Ambrosius, H. P. M. M.

, p. 344 - 346 (2007/10/02)

Phosphine derivatives containing a P-H bond can add to the C=N double bond of a hetero-allene molecule RN=C=X.Ph2PH gives Ph2PC(X)NHR (X = O, S: R = Ph; X = N-p-tol: R = p-tol), cy-C6H11Ph2 gives cy-C6H11P2 (X = O, S) and Ph2P(Q)H gives Ph2P(Q)C

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