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(4-Iodo-cyclohexyl)-carbaMic acid benzyl ester is a chemical compound that features a benzyl ester of carbaMic acid with a 4-iodo-cyclohexyl substituent. (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester is known for its utility in organic synthesis and holds potential in various fields, including pharmaceutical and agrochemical production, as well as material science and chemical research.

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  • 1353970-61-2 Structure
  • Basic information

    1. Product Name: (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester
    2. Synonyms: (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester
    3. CAS NO:1353970-61-2
    4. Molecular Formula: C14H18INO2
    5. Molecular Weight: 359.20269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1353970-61-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester(1353970-61-2)
    11. EPA Substance Registry System: (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester(1353970-61-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1353970-61-2(Hazardous Substances Data)

1353970-61-2 Usage

Uses

Used in Organic Synthesis:
(4-Iodo-cyclohexyl)-carbaMic acid benzyl ester is used as a reagent in organic synthesis for the creation of different chemical compounds. Its unique structure allows for versatile reactions and the formation of a wide range of products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester is used as a key intermediate in the synthesis of various drugs. Its presence in the molecular structure can contribute to the development of new medications with improved efficacy and reduced side effects.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester is utilized as an intermediate for the development of new pesticides, herbicides, and other agricultural chemicals, potentially enhancing crop protection and yield.
Used in Material Science:
(4-Iodo-cyclohexyl)-carbaMic acid benzyl ester may also find applications in material science, where its unique properties could be harnessed to create novel materials with specific characteristics, such as improved strength, durability, or chemical resistance.
Used in Chemical Research:
In the field of chemical research, (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester serves as a valuable compound for studying reaction mechanisms, exploring new synthetic pathways, and understanding the properties of related chemical structures.
Safety Note:
It is crucial to handle (4-Iodo-cyclohexyl)-carbaMic acid benzyl ester with care and follow all appropriate safety procedures when working with it in a laboratory setting to ensure the safety of both the researcher and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 1353970-61-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,9,7 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1353970-61:
(9*1)+(8*3)+(7*5)+(6*3)+(5*9)+(4*7)+(3*0)+(2*6)+(1*1)=172
172 % 10 = 2
So 1353970-61-2 is a valid CAS Registry Number.

1353970-61-2Upstream product

1353970-61-2Downstream Products

1353970-61-2Relevant articles and documents

Copper-Catalyzed Reductive Trifluoromethylation of Alkyl Iodides with Togni's Reagent

Chen, Yanchi,Ma, Guobin,Gong, Hegui

supporting information, p. 4677 - 4680 (2018/08/07)

This work illustrates a reductive cross-electrophile coupling protocol for trifluoromethylation of alkyl iodides under Cu-catalyzed/Ni-promoted reaction conditions. The use of diboron esters as the terminal reductant allows the effective generation of the alkyl-CF3 products with excellent functional group tolerance and broad substrate scope. A mechanism involving a reaction of alkyl-Cu with Togni's reagent was proposed.

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