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CAS

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93236-67-0

3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone is a 2-benzofuran consisting of phthalide with a butylidene group at the 3-position. It is a chemical compound that belongs to the class of isobenzofuranones and possesses a unique structure and properties.

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  • 93236-67-0 Structure

  • Basic information

    1. Product Name: 3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone
    2. Synonyms: (Z)-3-Butylidene-7-hydroxyisobenzofuran-1(3H)-one;3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone;Senkyunolide B;(Z)-3-butylidene-7-hydroxyphthalide
    3. CAS NO:93236-67-0
    4. Molecular Formula: C12H12O3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93236-67-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 375.3°C at 760 mmHg
    3. Flash Point: 165.5°C
    4. Appearance: /
    5. Density: 1.319g/cm3
    6. Vapor Pressure: 3.65E-06mmHg at 25°C
    7. Refractive Index: 1.666
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone(93236-67-0)
    12. EPA Substance Registry System: 3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone(93236-67-0)

  • 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: 93236-67-0(Hazardous Substances Data)

93236-67-0 Usage

Uses

Used in Pharmaceutical Industry:
3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone is used as a pharmaceutical compound for its potential therapeutic applications. Its unique structure and properties make it a promising candidate for the development of new drugs and treatments.
Used in Chemical Research:
3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone is used as a research compound in the field of organic chemistry. Its unique structure and properties make it an interesting subject for studying chemical reactions and mechanisms, as well as for the development of new synthetic methods and strategies.
Used in Material Science:
3-[(Z)-Butylidene]-7-hydroxy-1(3H)-isobenzofuranone can be used in material science for the development of new materials with specific properties. Its unique structure and properties can be exploited to create materials with applications in various fields, such as electronics, sensors, and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 93236-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,3 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93236-67:
(7*9)+(6*3)+(5*2)+(4*3)+(3*6)+(2*6)+(1*7)=140
140 % 10 = 0
So 93236-67-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O3/c1-2-3-7-10-8-5-4-6-9(13)11(8)12(14)15-10/h4-7,13H,2-3H2,1H3/b10-7-

93236-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-butylidene-7-hydroxyphthalide

1.2 Other means of identification

Product number -
Other names (3Z)-3-butylidene-7-hydroxy-2-benzofuran-1-one

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:93236-67-0 SDS

93236-67-0Downstream Products

93236-67-0Relevant articles and documents

Efficient Synthesis of Hydroxyphthalides

Ogawa, Yoshimitsu,Maruno, Masao,Wakamatsu, Takeshi

, p. 47 - 50 (2007/10/02)

Naturally occurring hydroxyphthalides were synthesized via migration of double bond regio- and stereoselectively.Isomerization of E-isomer to Z-isomer easily occurred under acidic or basic conditions.

Synthesis of 3-Butylidene-7-hydroxyphthalide

Mali, R.S.,Patil, S.R.

, p. 167 - 173 (2007/10/02)

A convenient synthesis of 3-butylidene-7-hydroxyphthalide (6) is described starting from 2-formyl-6-methoxybenzoic acid (1) via the intermediacy of iodophthalide (4).

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