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54315-44-5

Cyclohexanol, 1-[3-(diethylamino)-1-propynyl]-, acetate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54315-44-5 Structure

  • Basic information

    1. Product Name: Cyclohexanol, 1-[3-(diethylamino)-1-propynyl]-, acetate (ester)
    2. Synonyms:
    3. CAS NO:54315-44-5
    4. Molecular Formula: C15H25NO2
    5. Molecular Weight: 251.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54315-44-5.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: Cyclohexanol, 1-[3-(diethylamino)-1-propynyl]-, acetate (ester)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanol, 1-[3-(diethylamino)-1-propynyl]-, acetate (ester)(54315-44-5)
    11. EPA Substance Registry System: Cyclohexanol, 1-[3-(diethylamino)-1-propynyl]-, acetate (ester)(54315-44-5)

  • 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: 54315-44-5(Hazardous Substances Data)

54315-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54315-44-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,1 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54315-44:
(7*5)+(6*4)+(5*3)+(4*1)+(3*5)+(2*4)+(1*4)=105
105 % 10 = 5
So 54315-44-5 is a valid CAS Registry Number.

54315-44-5SDS

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-acetoxy-1-(3-diethylamino-1-propynyl)-cyclohexane

1.2 Other means of identification

Product number -
Other names 1-acetoxy-1-(3-diethylamino-prop-1-ynyl)-cyclohexane

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:54315-44-5 SDS

54315-44-5Relevant articles and documents

11,12-Secoprostaglandins

-

, (2008/06/13)

This invention relates to 11,12-secoprostaglandins and processes for their manufacture. These compounds have prostaglandin-like biological activity and are particularly useful as renal vasodilators, for the treatment of hypertension, for the prevention of thrombus formation, in preventing gastric secretion, and as regulators of the immune response.

8-Aza-9-oxo(and dioxo)-thia-11,12-secoprostaglandins

-

, (2008/06/13)

This invention relates to 8-aza-9-oxo(and dioxo)-thia-11,12-secoprostaglandins and processes for their manufacture. These compounds have prostaglandin-like biological activity and are particularly useful as renal vasodilators, for the prevention of thrombus formation, to induce growth hormone release, and as regulators of the immune response.

9-Thia- and oxothia- and 9-dioxothia-11,12-seco-prostaglandins and processes

-

, (2008/06/13)

This invention relates to 9-thia-, 9-oxothia, and 9-dioxothia-11,12-seco-prostaglandins and processes for their manufacture. These compounds have prostaglandin-like biological activity and are particularly useful for the treatment of skin diseases such as psoriasis, for the prevention of Thrombus formation, in stimulating the production of growth hormone in intact animals, and as regulators of the immune response.

11,12 Secoprostaglandins. 1. Acylhydroxyalkanoic acids and related compounds

Bicking,Robb,Smith,Cragoe Jr.

, p. 35 - 43 (2007/10/06)

The synthesis is described of a series of acylhydroxyalkanoic acids which embody structural modifications of that class of secoprostaglandins which are formally derived from the natural substances by scission of the cyclopentane ring between carbon atoms

11,12-Secoprostaglandins

-

, (2008/06/13)

This invention relates to 8,10-diaza-9-oxo(and thioxo)-11,12-secoprostaglandins and processes for their manufacture. These compounds have prostaglandin-like biological activity and are particularly useful as renal vasodilators, and for the prevention of thrombus formation.

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