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CAS

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78628-28-1

Roxatidine acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78628-28-1 Structure

  • Basic information

    1. Product Name: Roxatidine acetate
    2. Synonyms: ROXATIDINE ACETATE;2-(acetyloxy)-n-(3-(3-(1-piperidinylmethyl)phenoxy)propyl)-acetamid;2-(acetyloxy)-n-(3-(3-(1-piperidinylmethyl)phenoxy)propyl)acetamide;aceroxatidine;3-[3-(1-piperidylmethyl)phenoxy]propylcarbamoylmethyl acetate;2-(Acetyloxy)-N-[3-[3-(1-piperidinylmethyl)l~henoxy]19ropyl]acetamide;Altat：TZU-0460;Gastralgin：Roxit
    3. CAS NO:78628-28-1
    4. Molecular Formula: C19H28N2O4
    5. Molecular Weight: 348.43662
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78628-28-1.mol

  • Chemical Properties

    1. Melting Point: 59-60°
    2. Boiling Point: 537.3 °C at 760 mmHg
    3. Flash Point: 278.7 °C
    4. Appearance: white or off-white powder
    5. Density: 1.13 g/cm3
    6. Vapor Pressure: 1.29E-11mmHg at 25°C
    7. Refractive Index: 1.532
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: 14.23±0.46(Predicted)
    11. CAS DataBase Reference: Roxatidine acetate(CAS DataBase Reference)
    12. NIST Chemistry Reference: Roxatidine acetate(78628-28-1)
    13. EPA Substance Registry System: Roxatidine acetate(78628-28-1)

  • 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: 78628-28-1(Hazardous Substances Data)

78628-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78628-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,2 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78628-28:
(7*7)+(6*8)+(5*6)+(4*2)+(3*8)+(2*2)+(1*8)=171
171 % 10 = 1
So 78628-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C19H28N2O4/c1-16(22)25-15-19(23)20-9-6-12-24-18-8-5-7-17(13-18)14-21-10-3-2-4-11-21/h5,7-8,13H,2-4,6,9-12,14-15H2,1H3,(H,20,23)

78628-28-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-oxo-2-[3-[3-(piperidin-1-ylmethyl)phenoxy]propylamino]ethyl] acetate

1.2 Other means of identification

Product number -
Other names 2-(Acetyloxy)-N-(3-(3-(1-piperidinylmethyl)phenoxy)propyl)acetamide

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:78628-28-1 SDS

78628-28-1Downstream Products

78628-28-1Relevant articles and documents

Synthesis method of roxatidine acetate

-

, (2021/07/21)

The invention provides a preparation method of Roxatidine acetate, wherein the chemical name of the Roxatidine acetate is 2-acetoxy-N-[3-[3-(1-piperidinyl methyl) phenoxy] propyl] acetamide (formula VI). The method provided by the invention has the advantages of cheap and easily available raw materials, mild reaction conditions, high yield, simple post-treatment operation, green and environment-friendly solvent reagent and the like, reduces the cost, has certain technical advantages, is environment-friendly, and is suitable for large-scale industrial production.

The use of 2-hydroxymethyl benzoic acid as an effective water surrogate in the Passerini reaction: A straightforward access to α-hydroxyamides

Serafini, Marta,Griglio, Alessia,Oberto, Elena,Pirali, Tracey,Tron, Gian Cesare

, p. 4786 - 4789 (2017/11/29)

Dozens of strategies have been described for the synthesis of α-hydroxyamides over the years, but they share common drawbacks in terms of generality and tolerability, especially to acid labile functionalities. Here we report a truncated Passerini reaction suitable for the easy and mild preparation of functionalized α-hydroxyamides. In particular, this procedure is tolerant to acid sensitive protecting groups, which remain intact during the multicomponent reaction.

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