Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI) is a chemical compound with the molecular formula C8H12O2. It is an ester of cyclobutanecarboxylic acid, which is characterized by its four-membered ring structure. Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI) is known for its potential reactivity and toxicity, necessitating careful handling and adherence to proper safety guidelines.

40896-96-6 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 40896-96-6 Structure
  • Basic information

    1. Product Name: Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI)
    2. Synonyms: Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI);Ethyl 3-Methylenecyclobutanecarboxylate;3-Methylene-cyclobutanecarboxylic acid ethyl ester
    3. CAS NO:40896-96-6
    4. Molecular Formula: C8H12O2
    5. Molecular Weight: 140.17968
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICESTER
    8. Mol File: 40896-96-6.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: Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI)(40896-96-6)
    11. EPA Substance Registry System: Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI)(40896-96-6)
  • 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: 40896-96-6(Hazardous Substances Data)

40896-96-6 Usage

Uses

Used in Organic Synthesis:
Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI) is used as a reagent in organic synthesis for the preparation of various chemical compounds. Its unique four-membered ring structure and ester functionality make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Industrial Applications:
Although the specific industrial applications of Cyclobutanecarboxylic acid, 3-methylene-, ethyl ester (9CI) are not explicitly mentioned in the provided materials, its use in organic synthesis suggests that it may be employed in the production of various industrial chemicals or materials. Its potential reactivity and toxicity, however, must be considered when evaluating its suitability for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 40896-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,9 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40896-96:
(7*4)+(6*0)+(5*8)+(4*9)+(3*6)+(2*9)+(1*6)=146
146 % 10 = 6
So 40896-96-6 is a valid CAS Registry Number.

40896-96-6Downstream Products

40896-96-6Relevant articles and documents

NOVEL COMPOUNDS FOR USE IN CANCER

-

, (2019/01/07)

It relates to the compounds of formula (I), or their pharmaceutically or veterinary acceptable salts, or their stereoisomers or mixtures of stereoisomers, wherein X, L,R1, R 2, and R 3 are as defined herein, which are cancer cell differentiation inducing agents. It also relates to pharmaceutical or veterinary compositions containing them, and to their use in medicine, in particular in the treatment and/or prevention of cancer, in particular by cell differentiation therapy.

NOVEL COMPOUNDS FOR USE IN COGNITION IMPROVEMENT

-

, (2016/04/19)

Novel compounds for use in cognition improvement It relates to certain compounds having a polycyclic structure and a -(C=O)NRaRb moiety, wherein the polycyclic structure comprises at least three ring systems, wherein one ring system is a polycyclic ring system comprising from 2 to 4 rings; at least one ring is an aromatic ring; and wherein the structure comprises at least 3 nitrogen atoms and 1 oxygen atom. It also relates to pharmaceutical compositions containing them, and to their use in medicine, in particular in the treatment and/or prevention of neurological disorders coursing with a cognition deficit or impairment, or neurodegenerative diseases.

Design, Synthesis, and Biological Evaluation of First-in-Class Dual Acting Histone Deacetylases (HDACs) and Phosphodiesterase 5 (PDE5) Inhibitors for the Treatment of Alzheimer's Disease

Rabal, Obdulia,Sánchez-Arias, Juan A.,Cuadrado-Tejedor, Mar,De Miguel, Irene,Pérez-González, Marta,García-Barroso, Carolina,Ugarte, Ana,Estella-Hermoso De Mendoza, Ander,Sáez, Elena,Espelosin, Maria,Ursua, Susana,Haizhong, Tan,Wei, Wu,Musheng, Xu,Garcia-Osta, Ana,Oyarzabal, Julen

, p. 8967 - 9004 (2016/10/22)

Simultaneous inhibition of phosphodiesterase 5 (PDE5) and histone deacetylases (HDAC) has recently been validated as a potentially novel therapeutic approach for Alzheimer's disease (AD). To further extend this concept, we designed and synthesized the first chemical series of dual acting PDE5 and HDAC inhibitors, and we validated this systems therapeutics approach. Following the implementation of structure- and knowledge-based approaches, initial hits were designed and were shown to validate our hypothesis of dual in vitro inhibition. Then, an optimization strategy was pursued to obtain a proper tool compound for in vivo testing in AD models. Initial hits were translated into molecules with adequate cellular functional responses (histone acetylation and cAMP/cGMP response element-binding (CREB) phosphorylation in the nanomolar range), an acceptable therapeutic window (>1 log unit), and the ability to cross the blood-brain barrier, leading to the identification of 7 as a candidate for in vivo proof-of-concept testing (Cuadrado-Tejedor, M.; Garcia-Barroso, C.; Sánchez-Arias, J. A.; Rabal, O.; Mederos, S.; Ugarte, A.; Franco, R.; Segura, V.; Perea, G.; Oyarzabal, J.; Garcia-Osta, A. Neuropsychopharmacology 2016, in press, doi: 10.1038/npp.2016.163).

NOVEL COMPOUNDS AS DUAL INHIBITORS OF PHOSPHODIESTERASES AND HISTONE DEACETYLASES

-

Page/Page column 74; 75, (2014/09/16)

It relates to certain compounds having a polycyclic structure and a hydroxamic acid moiety, wherein the polycyclic structure comprises at least three ring systems, wherein one ring system is a polycyclic ring system comprising from 2 to 4 rings; at least one ring is an aromatic ring; and wherein the structure comprises at least 3 nitrogen atoms and 1 oxygen atom. It also relates to a process for their preparation, as well as to pharmaceutical compositions containing them, and to their use in medicine, in particular in the treatment and/or prevention of neurological disorders coursing with a cognition deficit or impairment, or neurodegenerative diseases. wherein B1 is a radical selected from the group consisting of formula (A"), formula (B"), formula (C"), and formula (D"):

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

What can I do for you?
Get Best Price

Get Best Price for 40896-96-6