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178242-93-8

4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER is a chemical compound with the molecular formula C8H13NO3. It is an ester derivative of 4-amino-tetrahydropyran-4-acetic acid, known for its structural properties and reactivity. 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER plays a significant role in organic synthesis and pharmaceutical research, with potential applications in the development of new drugs and pharmaceuticals.

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  • 178242-93-8 Structure

  • Basic information

    1. Product Name: 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER
    2. Synonyms: 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER ;methyl 2-(4-aminotetrahydro-2H-pyran-4-yl)acetate;REF DUPL: Methyl DL-2-(tetrahydropyran-4-yl)-beta-glycinate;2H-Pyran-4-acetic acid, 4-aminotetrahydro-, methyl ester
    3. CAS NO:178242-93-8
    4. Molecular Formula: C8H15NO3
    5. Molecular Weight: 173.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 178242-93-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 241°C at 760 mmHg
    3. Flash Point: 91.5°C
    4. Appearance: /
    5. Density: 1.075g/cm3
    6. Vapor Pressure: 0.0367mmHg at 25°C
    7. Refractive Index: 1.456
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER(178242-93-8)
    12. EPA Substance Registry System: 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER(178242-93-8)

  • 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: 178242-93-8(Hazardous Substances Data)

178242-93-8 Usage

Uses

Used in Pharmaceutical Research and Development:
4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block for creating new drug molecules with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic synthesis, 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER is utilized as a reagent or a precursor for the preparation of a wide range of organic compounds. Its reactivity and functional groups make it suitable for various chemical reactions, contributing to the synthesis of complex organic molecules.
Used in Drug Discovery:
4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER is employed as a potential pharmacological agent in drug discovery. Its structural properties and reactivity have been studied for their potential to treat various medical conditions, making it a promising candidate for further research and development in the pharmaceutical industry.
Overall, 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER is a versatile and important chemical compound with a wide range of potential applications in various fields, including pharmaceutical research, organic synthesis, and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 178242-93-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,2,4 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 178242-93:
(8*1)+(7*7)+(6*8)+(5*2)+(4*4)+(3*2)+(2*9)+(1*3)=158
158 % 10 = 8
So 178242-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO3/c1-11-7(10)6-8(9)2-4-12-5-3-8/h2-6,9H2,1H3

178242-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-AMINO-TETRAHYDROPYRAN-4-ACETIC ACID METHYL ESTER

1.2 Other means of identification

Product number -
Other names methyl 2-(4-aminotetrahydro-2H-pyran-4-yl)acetate

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:178242-93-8 SDS

178242-93-8Relevant articles and documents

PARTIALLY SATURATED NITROGEN-CONTAINING HETEROCYCLIC COMPOUND

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Paragraph 0253, (2015/06/17)

There are provided compounds having a superior PHD2 inhibitory effect that are represented by general formula (I'): (in the above-mentioned general formula (I'), W, Y, R2, R3, R4, and Y4 are as described hereinabove), or pharmaceutically acceptable salts thereof.

Synthesis and structure-activity relationship of a novel, achiral series of TNF-α converting enzyme inhibitors

Gilmore, John L.,King, Bryan W.,Harris, Cathy,Maduskuie, Thomas,Mercer, Stephen E.,Liu, Rui-Qin,Covington, Maryanne B.,Qian, Mingxin,Ribadeneria, Maria D.,Vaddi, Krishna,Trzaskos, James M.,Newton, Robert C.,Decicco, Carl P.,Duan, James J.-W.

, p. 2699 - 2704 (2007/10/03)

A novel series of achiral TNF-α converting enzyme (TACE) inhibitors has been discovered. These compounds exhibited activities from 0.35 to 11 nM in a porcine TACE assay and inhibited TNF-α production in an LPS-stimulated whole blood assay with an IC5

Novel 5-hydroxytryptamine 4 (5-HT4) receptor agonists. Synthesis and gastroprokinetic activity of 4-amino-N-[2-(1-aminocycloalkan-1-yl)ethyl]-5- chloro-2-methoxybenzamides

Suzuki, Takeshi,Imanishi, Naoki,Itahana, Hirotsune,Watanuki, Susumu,Miyata, Keiji,Ohta, Mitsuaki,Nakahara, Hideaki,Yamagiwa, Yoko,Mase, Toshiyasu

, p. 1116 - 1124 (2007/10/03)

A novel series of 4-amino-N-[2-(1-aminocycloalkan-1-yl)ethyl]-5-chloro- 2-methoxybenzamide derivatives (1), which had amines conformationally restricted due to the effect of repulsion by neighboring substituents, were prepared and evaluated for 5-hydroxytryptamine 4 (5-HT4) agonistic activities by using the contraction of longitudinal muscle myenteric plexus (LMMP) of guinea pig ileum. One of the most potent compounds in this series was 4-amino-5-chloro-N-[2-(1-dimethylamino-1-cyclohexyl)ethyl]-2- methoxybenzamide (1c, YM-47813) with an EC50 value of 1.0 μM on LMMP. This compound effectively enhanced gastric motility and gastric emptying in conscious dogs by oral administration (1-3 mg/kg).

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