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2-Furancarboxylicacid,tetrahydro-2-(2-propenyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 267425-71-8 Structure
  • Basic information

    1. Product Name: 2-Furancarboxylicacid,tetrahydro-2-(2-propenyl)-(9CI)
    2. Synonyms: 2-Furancarboxylicacid,tetrahydro-2-(2-propenyl)-(9CI);allyl tetrahydrofuran-2-carboxylate
    3. CAS NO:267425-71-8
    4. Molecular Formula: C8H12O3
    5. Molecular Weight: 156.17908
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICACID
    8. Mol File: 267425-71-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 267.0±33.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.118±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.58±0.20(Predicted)
    10. CAS DataBase Reference: 2-Furancarboxylicacid,tetrahydro-2-(2-propenyl)-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Furancarboxylicacid,tetrahydro-2-(2-propenyl)-(9CI)(267425-71-8)
    12. EPA Substance Registry System: 2-Furancarboxylicacid,tetrahydro-2-(2-propenyl)-(9CI)(267425-71-8)
  • 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: 267425-71-8(Hazardous Substances Data)

267425-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 267425-71-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,7,4,2 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 267425-71:
(8*2)+(7*6)+(6*7)+(5*4)+(4*2)+(3*5)+(2*7)+(1*1)=158
158 % 10 = 8
So 267425-71-8 is a valid CAS Registry Number.

267425-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-allyl-2-tetrahydrofuroic acid

1.2 Other means of identification

Product number -
Other names (S)-2-Allyl-tetrahydro-furan-2-carboxylic 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:267425-71-8 SDS

267425-71-8Relevant articles and documents

Palladium-Catalyzed Alkene Carboalkoxylation Reactions of Phenols and Alcohols for the Synthesis of Carbocycles

White, Derick R.,Herman, Madeline I.,Wolfe, John P.

supporting information, p. 4311 - 4314 (2017/08/23)

Intermolecular alkene difunctionalization reactions between terminal alkenes bearing a pendant aryl or alkenyl triflate electrophile and exogenous alcohol or phenol nucleophiles are described. These transformations afford substituted indanyl or alkylidene

Heterocycle amides as cell adhesion inhibitors

-

, (2008/06/13)

Compounds of Formula I are antagonists of VLA-4 and/or α4β7, and as such are useful in the inhibition or prevention of cell adhesion and cell-adhesion mediated pathologies. These compounds may be formulated into pharmaceutical compositions and are suitable for use in the treatment of AIDS-related dementia, allergic conjunctivitis, allergic rhinitis, Alzheimer's disease, asthma, atherosclerosis, autologous bone marrow transplantation, certain types of toxic and immune-based nephritis, contact dermal hypersensitivity, inflammatory bowel disease including ulcerative colitis and Crohn's disease, inflammatory lung diseases, inflammatory sequelae of viral infections, meningitis, multiple sclerosis, multiple myeloma, myocarditis, organ transplantation, psoriasis, pulmonary fibrosis, restenosis, retinitis, rheumatoid arthritis, septic arthritis, stroke, tumor metastasis, uveititis, and type I diabetes.

Synthesis of (-)-dysiherbaine.

Snider,Hawryluk

, p. 635 - 638 (2007/10/03)

[reaction: see text] The first synthesis of (-)-dysiherbaine has been accomplished using intramolecular SN2 substitutions of a carbamate anion on an epoxide and an alkoxide on a secondary mesylate to efficiently construct the bicyclic skeleton stereospecifically from xylose. A general sequence has been developed to introduce an allyl group and convert it to the alanine side chain that should be useful for the construction of dysiherbaine analogues.

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