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

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  • 51112-81-3 Structure
  • Basic information

    1. Product Name: endoxo-delta(4)-tetrahydrophthalic acid
    2. Synonyms: endoxo-delta(4)-tetrahydrophthalic acid
    3. CAS NO:51112-81-3
    4. Molecular Formula: C8H8O5
    5. Molecular Weight: 184.14612
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 51112-81-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 464.5°Cat760mmHg
    3. Flash Point: 199.1°C
    4. Appearance: /
    5. Density: 1.614g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.53±0.40(Predicted)
    10. CAS DataBase Reference: endoxo-delta(4)-tetrahydrophthalic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: endoxo-delta(4)-tetrahydrophthalic acid(51112-81-3)
    12. EPA Substance Registry System: endoxo-delta(4)-tetrahydrophthalic acid(51112-81-3)
  • 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: 51112-81-3(Hazardous Substances Data)

51112-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51112-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,1 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51112-81:
(7*5)+(6*1)+(5*1)+(4*1)+(3*2)+(2*8)+(1*1)=73
73 % 10 = 3
So 51112-81-3 is a valid CAS Registry Number.

51112-81-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (endo,endo)-7-Oxabicyclo(2.2.1)hept-5-ene-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:51112-81-3 SDS

51112-81-3Relevant articles and documents

Supramolecular chemistry under mechanochemical conditions: A small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction

MacGillivray, Leonard R.,Swenson, Dale C.,Yelgaonkar, Shweta P.

, p. 3569 - 3573 (2020)

We describe the integration of a small-molecule hydrogen-bond-donor template into a cascade reaction that is comprised of a combination of molecular and supramolecular events. The cascade is performed mechanochemically and in the presence of μL amounts of

METHOD FOR THE PREPARATION OF FUSED HETEROCYCLIC SUCCINIMIDE COMPOUNDS AND ANALOGS THEREOF

-

, (2008/06/13)

Fused cyclic compounds, methods of using such compounds in the treatment of nuclear hormone receptor-associated conditions such as cancer and immune disorders, and pharmaceutical compositions containing such compounds.

Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function

-

, (2008/06/13)

Fused cyclic compounds, methods of using such compounds in the treatment of nuclear hormone receptor-associated conditions such as cancer and immune disorders, and pharmaceutical compositions containing such compounds.

PROCESS FOR PREPARATION OF 7-OXABICYCLO[2.2.1]HEPT-5-ENE-2-CARBOXYLIC ACID DERIVATIVES

-

, (2008/06/13)

The present invention provides a method of industrially advantageously producing 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylic acid derivatives under mild conditions in a high yield. The present invention relates to a production method of a 7-oxabicyclo[2.2.1]hept-5-ene-2-carboxylic acid derivative of the formula (III) or the formula (IV), which comprises reacting an α,β-unsaturated carboxylic acid of the formula (I) with a furan derivative of the formula (II) in the presence of a Lewis acid: wherein each symbol is as defined in the specification.

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