Welcome to LookChem.com Sign In|Join Free
  • or
3-[3-(Dimethylamino)propoxy]benzaldehyde, also known as AMPSO Formaldehyde, is an organic compound with the molecular formula C13H19NO2. It is a pale yellow liquid that is commonly used as an intermediate in the synthesis of pharmaceuticals and other chemicals. Its chemical structure contains a benzene ring with an aldehyde group and a propoxy group, as well as a dimethylamino group, which gives it its unique chemical properties. AMPSO Formaldehyde typically has a strong, aromatic odor and is considered to be a hazardous chemical, requiring careful handling and storage.

26815-13-4

Post Buying Request

26815-13-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

26815-13-4 Usage

Uses

Used in Pharmaceutical Industry:
3-[3-(Dimethylamino)propoxy]benzaldehyde is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be a key building block in the production of organic compounds.
Used in Chemical Industry:
3-[3-(Dimethylamino)propoxy]benzaldehyde is used as a raw material in the production of dyes, perfumes, and agricultural chemicals due to its unique chemical properties and versatility in organic synthesis.
Used in Research and Development:
3-[3-(Dimethylamino)propoxy]benzaldehyde is utilized in research and development for the exploration of new chemical reactions and the creation of novel organic compounds, given its potential as a key building block in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 26815-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,1 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26815-13:
(7*2)+(6*6)+(5*8)+(4*1)+(3*5)+(2*1)+(1*3)=114
114 % 10 = 4
So 26815-13-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO2/c1-13(2)7-4-8-15-12-6-3-5-11(9-12)10-14/h3,5-6,9-10H,4,7-8H2,1-2H3

26815-13-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[3-(dimethylamino)propoxy]benzaldehyde

1.2 Other means of identification

Product number -
Other names BB_SC-5718

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:26815-13-4 SDS

26815-13-4Relevant academic research and scientific papers

Design and synthesis of benzylpiperidine inhibitors targeting the menin–MLL1 interface

Ren, Jing,Xu, Wei,Tang, Le,Su, Minbo,Chen, Danqi,Chen, Yue-Lei,Zang, Yi,Li, Jia,Shen, Jingkang,Zhou, Yubo,Xiong, Bing

supporting information, p. 4472 - 4476 (2016/08/25)

Menin is an essential oncogenic cofactor for mixed lineage leukemia (MLL)-mediated leukemogenesis, functioning through its direct interaction with MLL1 protein. Therefore, targeting the menin–MLL1 protein–protein interface represents a promising strategy

Synthesis, cytotoxicity and topoisomerase inhibition properties of multifarious aminoalkylated indeno[1,2-c]isoquinolin-5,11-diones

Ahn, Gang,Schifano-Faux, Nadège,Goossens, Jean-Fran?ois,Baldeyrou, Brigitte,Couture, Axel,Grandclaudon, Pierre,Lansiaux, Amélie,Ryckebusch, Adina

scheme or table, p. 2259 - 2263 (2011/05/15)

A number of mono- or diaminoalkylated indeno[1,2-c]isoquinolin-5,11-diones analogs of 1 were synthesized and evaluated for their DNA binding affinities, topoisomerase inhibition properties and antiproliferative activities against human cancer cell lines (

Aryl-substituted benzimidazole and imidazopyridine ethers

-

Page/Page column 14, (2010/02/15)

Aryl substituted benzimidazole and imidazo[4,5]pyridine ethers are described as inhibitors of Cds1 and useful as adjuvants to chemotherapy or radiation therapy in the treatment of cancer.

Butenolide endothelin antagonists with improved aqueous solubility

Patt, William C.,Cheng, Xue-Min,Repine, Joseph T.,Lee, Chet,Reisdorph, Bill R.,Massa, Mark A.,Doherty, Annette M.,Welch, Kathleen M.,Bryant, John W.,Flynn, Michael A.,Walker, Donnelle M.,Schroeder, Richard L.,Haleen, Stephen J.,Keiser, Joan A.

, p. 2162 - 2168 (2007/10/03)

Continued development around our ET(A)-selective endothelin (ET) antagonist 1 (CI-1020) has led to the synthesis of analogues with improved aqueous solubility profiles. Poor solubility characteristics displayed by 1 required a complex buffered formulation

CNS active compounds

-

, (2008/06/13)

Compounds of the formula SPC1 Wherein X, R, n and B are as defined herein exhibit antidepressant activity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 26815-13-4