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5-aminovaleric acid hydroiodide is a chemical compound that belongs to the class of amino acids. It is a derivative of valeric acid and contains an amino group, making it a valuable intermediate in organic synthesis. 5-aminovaleric acid hydroiodide is known for its ability to react with other chemicals to form new compounds with diverse biological activities and is commonly used in pharmaceutical research and development as a building block for the synthesis of various drugs and biologically active compounds. It is also used as a reagent in organic chemistry for the preparation of various organic molecules and pharmaceuticals.

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  • 1705581-28-7 Structure
  • Basic information

    1. Product Name: 5-aminovaleric acid hydroiodide
    2. Synonyms:
    3. CAS NO:1705581-28-7
    4. Molecular Formula:
    5. Molecular Weight: 245.06
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1705581-28-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-aminovaleric acid hydroiodide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-aminovaleric acid hydroiodide(1705581-28-7)
    11. EPA Substance Registry System: 5-aminovaleric acid hydroiodide(1705581-28-7)
  • 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: 1705581-28-7(Hazardous Substances Data)

1705581-28-7 Usage

Uses

Used in Pharmaceutical Research and Development:
5-aminovaleric acid hydroiodide is used as a building block for the synthesis of various drugs and biologically active compounds. Its unique structure allows it to be incorporated into the design and synthesis of new pharmaceutical agents, potentially leading to the discovery of novel therapeutics.
Used in Organic Synthesis:
5-aminovaleric acid hydroiodide is used as a valuable intermediate in organic synthesis. Its ability to react with other chemicals enables the formation of new compounds with diverse biological activities, contributing to the development of innovative organic molecules and pharmaceuticals.
Used in Organic Chemistry as a Reagent:
5-aminovaleric acid hydroiodide serves as a reagent in organic chemistry for the preparation of various organic molecules and pharmaceuticals. Its versatility in reactions facilitates the synthesis of a wide range of compounds, enhancing the scope of organic chemistry research and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1705581-28-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,5,5,8 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1705581-28:
(9*1)+(8*7)+(7*0)+(6*5)+(5*5)+(4*8)+(3*1)+(2*2)+(1*8)=167
167 % 10 = 7
So 1705581-28-7 is a valid CAS Registry Number.

1705581-28-7Upstream product

1705581-28-7Downstream Products

1705581-28-7Relevant articles and documents

Improved Performance of Printable Perovskite Solar Cells with Bifunctional Conjugated Organic Molecule

Hu, Yue,Zhang, Zhihui,Mei, Anyi,Jiang, Youyu,Hou, Xiaomeng,Wang, Qifei,Du, Kai,Rong, Yaoguang,Zhou, Yinhua,Xu, Gengzhao,Han, Hongwei

, (2018)

A bifunctional conjugated organic molecule 4-(aminomethyl) benzoic acid hydroiodide (AB) is designed and employed as an organic cation in organic–inorganic halide perovskite materials. Compared with the monofunctional cation benzylamine hydroiodide (BA) and the nonconjugated bifunctional organic molecule 5-ammonium valeric acid, devices based on AB-MAPbI3 show a good stability and a superior power conversion efficiency of 15.6% with a short-circuit current of 23.4 mA cm?2, an open-circuit voltage of 0.94 V, and a fill factor of 0.71. The bifunctional conjugated cation not only benefits the growth of perovskite crystals in the mesoporous network, but also facilitates the charge transport. This investigation helps explore new approaches to rational design of novel organic cations for perovskite materials.

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