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CAS

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96325-10-9

(+/-)-2-[(benzyloxy)carbonyl]-1,3-dihydro-2H-isoindole-1-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 96325-10-9 Structure

  • Basic information

    1. Product Name: (+/-)-2-[(benzyloxy)carbonyl]-1,3-dihydro-2H-isoindole-1-carboxylic acid
    2. Synonyms: (+/-)-2-[(benzyloxy)carbonyl]-1,3-dihydro-2H-isoindole-1-carboxylic acid
    3. CAS NO:96325-10-9
    4. Molecular Formula:
    5. Molecular Weight: 297.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96325-10-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (+/-)-2-[(benzyloxy)carbonyl]-1,3-dihydro-2H-isoindole-1-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-2-[(benzyloxy)carbonyl]-1,3-dihydro-2H-isoindole-1-carboxylic acid(96325-10-9)
    11. EPA Substance Registry System: (+/-)-2-[(benzyloxy)carbonyl]-1,3-dihydro-2H-isoindole-1-carboxylic acid(96325-10-9)

  • 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: 96325-10-9(Hazardous Substances Data)

96325-10-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The compound is a solid at room temperature and appears white in color.

Explanation

It is commonly used as a reagent in the synthesis of various compounds in the field of organic chemistry.

Explanation

These functional groups make the compound useful for the modification of other molecules through chemical reactions.

Explanation

The presence of an isoindole ring in the compound gives it unique properties and potential applications in pharmaceutical research and manufacturing.

Explanation

The compound should be handled with caution, as it can be harmful if ingested or inhaled.

Explanation

To minimize the risk of exposure, the compound should be used in a well-ventilated area, and appropriate personal protective equipment (such as gloves, goggles, and a mask) should be worn.

Physical state

White solid

Usage

Reagent in organic chemistry

Functional groups

Carboxylic acid group, carbonyl group, and benzyl ether group

Structural feature

Isoindole ring

Safety precautions

Toxic if ingested or inhaled

Handling guidelines

Use in a well-ventilated area with appropriate personal protective equipment

Check Digit Verification of cas no

The CAS Registry Mumber 96325-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,2 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96325-10:
(7*9)+(6*6)+(5*3)+(4*2)+(3*5)+(2*1)+(1*0)=139
139 % 10 = 9
So 96325-10-9 is a valid CAS Registry Number.

96325-10-9SDS

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 2H-Isoindole-1,2-dicarboxylic acid, 1,3-dihydro-, 2-(phenylmethyl) ester

1.2 Other means of identification

Product number -
Other names N-Cbz-isoindoline-1-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:96325-10-9 SDS

96325-10-9Downstream Products

96325-10-9Relevant articles and documents

Dynamic kinetic resolution of 1,3-dihydro-2 h-isoindole-1-carboxylic acid methyl ester: Asymmetric transformations toward isoindoline carbamates

Moran-Ramallal, Roberto,Gotor-Fernandez, Vicente,Laborda, Pedro,Sayago, Francisco J.,Cativiela, Carlos,Gotor, Vicente

, p. 1696 - 1699 (2012/06/29)

Asymmetric syntheses of isoindoline carbamates have been successfully achieved through enzyme-mediated dynamic kinetic resolution processes and without requirement of metal or acid-base catalyst for the substrate racemization. Optically active carbamates

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