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164648-76-4

4-(aminomethyl)-N,N-dimethylbenzamide(SALTDATA: 1.27HCl 0.45H2O) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 164648-76-4 Structure

  • Basic information

    1. Product Name: 4-(aminomethyl)-N,N-dimethylbenzamide(SALTDATA: 1.27HCl 0.45H2O)
    2. Synonyms: 4-(aminomethyl)-N,N-dimethylbenzamide(SALTDATA: 1.27HCl 0.45H2O)
    3. CAS NO:164648-76-4
    4. Molecular Formula: C10H14N2O
    5. Molecular Weight: 178.23096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 164648-76-4.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: 4-(aminomethyl)-N,N-dimethylbenzamide(SALTDATA: 1.27HCl 0.45H2O)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(aminomethyl)-N,N-dimethylbenzamide(SALTDATA: 1.27HCl 0.45H2O)(164648-76-4)
    11. EPA Substance Registry System: 4-(aminomethyl)-N,N-dimethylbenzamide(SALTDATA: 1.27HCl 0.45H2O)(164648-76-4)

  • 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: 164648-76-4(Hazardous Substances Data)

164648-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164648-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,6,4 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 164648-76:
(8*1)+(7*6)+(6*4)+(5*6)+(4*4)+(3*8)+(2*7)+(1*6)=164
164 % 10 = 4
So 164648-76-4 is a valid CAS Registry Number.

164648-76-4Downstream Products

164648-76-4Relevant articles and documents

Rapid and Selective Cleavage of Amide Groups at Neutral pH: Applications from Hyaluronic Acid to Small Molecules

Jing, Jing,Bankefors, Johan,Bonneaud, Céline,Sawen, Elin,Gerfaud, Thibaud,Westin, Jonatan,El-Bazbouz, Ghizlane,Kandelin, Lina,Rousseau, Antoine,Olsson, Johan,Karlsson, Anders,Nord, Lars,Bouix-Peter, Claire,Helander Kenne, Anne,Boiteau, Jean-Guy,Tomas, Loic,Hennequin, Laurent,Harris, Craig S.

supporting information, p. 2995 - 3000 (2018/06/27)

During our investigation to find suitable conditions to prepare very high molecular weight partially de-acetylated hyaluronic acid (HA), we discovered a powerful new method to cleave amide bonds using hydroxylamine salts at neutral pH with remarkable sele

Improved syntheses of 5′- S -(2-Aminoethyl)-6- N -(4-nitrobenzyl)- 5′-thioadenosine (SAENTA), analogues, and fluorescent probe conjugates: Analysis of cell-surface human equilibrative nucleoside transporter 1 (hENT1) levels for prediction of the antitumor

Robins, Morris J.,Peng, Yunshan,Damaraju, Vijaya L.,Mowles, Delores,Barron, Geraldine,Tackaberry, Tracey,Young, James D.,Cass, Carol E.

experimental part, p. 6040 - 6053 (2010/11/02)

5′-S-(2-Aminoethyl)-6-N-(4-nitrobenzyl)-5′-thioadenosine (SAENTA), 5′-S-(2-acetamidoethyl)-6-N-[(4-substituted)benzyl]-5′- thioadenosine analogues, 5′-S-[2-(6-aminohexanamido)]ethyl-6-N-(4- nitrobenzyl)-5′-thioadenosine (SAHENTA), and related compounds we

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