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4-(Diethylamino)butyric acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63867-13-0 Structure
  • Basic information

    1. Product Name: 4-(Diethylamino)butyric acid
    2. Synonyms: 4-(Diethylamino)butyric acid;DF-472
    3. CAS NO:63867-13-0
    4. Molecular Formula: C8H17NO2
    5. Molecular Weight: 159.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63867-13-0.mol
  • Chemical Properties

    1. Melting Point: 166 °C
    2. Boiling Point: 255.1°Cat760mmHg
    3. Flash Point: 108.1°C
    4. Appearance: /
    5. Density: 0.98g/cm3
    6. Vapor Pressure: 0.00511mmHg at 25°C
    7. Refractive Index: 1.458
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 4.42±0.10(Predicted)
    11. CAS DataBase Reference: 4-(Diethylamino)butyric acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: 4-(Diethylamino)butyric acid(63867-13-0)
    13. EPA Substance Registry System: 4-(Diethylamino)butyric acid(63867-13-0)
  • 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: 63867-13-0(Hazardous Substances Data)

63867-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63867-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,6 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63867-13:
(7*6)+(6*3)+(5*8)+(4*6)+(3*7)+(2*1)+(1*3)=150
150 % 10 = 0
So 63867-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO2/c1-3-9(4-2)7-5-6-8(10)11/h3-7H2,1-2H3,(H,10,11)

63867-13-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(N,N-diethylamino)butanoic acid

1.2 Other means of identification

Product number -
Other names 4-diethylamino-butyric acid

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:63867-13-0 SDS

63867-13-0Relevant articles and documents

Carbamate as an accelerating group in intermolecular Pauson-Khand reaction

Asano, Shota,Itto-Nakama, Kaori,Arimoto, Hirokazu

supporting information, (2020/05/05)

The Pauson-Khand reaction (PKR) is a powerful means for the construction of cyclopentenones. However, its applications have been limited to the intramolecular version of this reaction because poor yield and regioselectivity are often the major problems in intermolecular PKR. Here we describe that a carbamate moiety in alkene substrate accelerates this intermolecular PKR. The reaction of N-4-dimethylaminophenyl O-allyl carbamate with alkyne-cobalt complex gave cyclopentenones in high yield (up to 90%) and regioselectivity (>9:1).

LIPIDS AND LIPID COMPOSITIONS FOR THE DELIVERY OF ACTIVE AGENTS

-

Page/Page column 94, (2016/03/19)

This invention provides for a compound of formula (I), or a pharmaceutically acceptable salt thereof, wherein RA, RB, R2 and R4 are defined herein. The compounds of formula (I) and pharmaceutically acceptable salts thereof are cationic lipids useful in the delivery of biologically active agents to cells and tissues.

Pharmaceutical composition containing quinoline or quinazoline derivatives and derivatives therefor

-

, (2008/06/13)

This invention provides an anti-inflammatory agent, particularly an agent for treating arthritis, containing a quinoline or quinazoline derivative or a salt thereof STR1 wherein Y is a nitrogen atom or C--G in which G is an optionally esterified carboxyl group;R 1 and R 2 are each independently a hydrogen atom, optionally substituted hydrocarbon group or optionally substituted heterocyclic group, or R 1 and R 2 are linked together to form a saturated ring;each of the ring A and ring B may optionally be substituted;n is an integer of 1 to 4; andk is 0 or 1.This invention also provides a novel quinoline or quinazoline derivative having anti-inflammatory activity.

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