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2-Pentanol,5-(diethylamino)-,(2S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 415679-46-8 Structure
  • Basic information

    1. Product Name: 2-Pentanol,5-(diethylamino)-,(2S)-(9CI)
    2. Synonyms: 2-Pentanol,5-(diethylamino)-,(2S)-(9CI)
    3. CAS NO:415679-46-8
    4. Molecular Formula: C9H21NO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 415679-46-8.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: 2-Pentanol,5-(diethylamino)-,(2S)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Pentanol,5-(diethylamino)-,(2S)-(9CI)(415679-46-8)
    11. EPA Substance Registry System: 2-Pentanol,5-(diethylamino)-,(2S)-(9CI)(415679-46-8)
  • 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: 415679-46-8(Hazardous Substances Data)

415679-46-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 415679-46-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,5,6,7 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 415679-46:
(8*4)+(7*1)+(6*5)+(5*6)+(4*7)+(3*9)+(2*4)+(1*6)=168
168 % 10 = 8
So 415679-46-8 is a valid CAS Registry Number.

415679-46-8Relevant articles and documents

The effects of a hydroxyl group on some chemical and biological properties of n-pentyl ammonium salts

Barlow

, p. 703 - 710 (1978)

The effects of a hydroxyl group on the activity and affinity of compounds related to n-pentyltrimethylammonium have been studied on the guinea pig ileum, frog rectus, acetylcholinesterase and on partitioning (Rm) and size (Φ(v0), Vm). The hydroxyl group lowered affinity in all tests, confirming the importance of hydrophobic forces in binding to receptors. Activity on the ileum was lowered appreciably but on the rectus only slightly. The effects on Rm did not indicate any interactions between hydroxyl, onium group and water but the apparent size of the hydroxyl group (ΔΦ(v0)) depends on the nature of the onium group.

Reductive hydroxyalkylation/alkylation of amines with lactones/esters

Wang, Yu-Huang,Ye, Jian-Liang,Wang, Ai-E,Huang, Pei-Qiang

, p. 6504 - 6511 (2012/09/08)

We have developed a one-pot method for the direct intermolecular reductive hydroxyalkylation or alkylation of amines using lactones or esters as the hydroxyalkylating/alkylating reagents. The method is based on the in situ amidation of lactones/esters with DIBAL-H-amine complex (for primary amines) or DIBAL-H-amine hydrochloride salt complex (for secondary amines), followed by reduction of the amides with an excess of DIBAL-H. Different from the reduction of Weinreb amides with DIBAL-H where aldehydes are formed, the reduction of the in situ formed Weinreb amides yielded amines. Moreover, this method is not limited to Weinreb amides, instead, it also works for other amides in general. A plausible mechanism is suggested to account for the outcome of the reactions.

Detritylation Procedure under Non-Acidic Conditions: Naphthalene Catalysed Reductive Cleavage of Trityl Ethers

Yus, Miguel,Behloul, Cherif,Guijarro, David

, p. 2179 - 2184 (2007/10/03)

The reaction of primary, secondary, allylic and benzylic trityl ethers 1 with lithium powder and a catalytic amount of naphthalene led to reductive cleavage of the trityl-oxygen bond, affording the corresponding alcohols 2 in good to excellent yields under very mild reaction conditions. The detritylation process could successfully be extended to several hydroxy, alkoxy and amino functionalised trityl ethers. This methodology represents a new and efficient detritylation procedure under non-acidic reaction conditions.

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