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85262-96-0

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85262-96-0 Usage

Physical state

Colorless, volatile liquid

Odor

Sweet, floral

Usage

Flavoring and fragrance agent in food and cosmetic industries

Synthesis

Esterification of 1,3-benzodioxole-5-carboxylic acid with methanol

Natural occurrence

Found in certain plants

Antimicrobial properties

Acts as a preservative in various products

Antioxidant properties

Helps prevent oxidation in products

Potential irritant

Can cause skin and eye irritation

Sensitizing effects

May cause sensitization on skin and eyes

Handling precautions

Should be handled with care to avoid skin and eye contact

Check Digit Verification of cas no

The CAS Registry Mumber 85262-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,6 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85262-96:
(7*8)+(6*5)+(5*2)+(4*6)+(3*2)+(2*9)+(1*6)=150
150 % 10 = 0
So 85262-96-0 is a valid CAS Registry Number.

85262-96-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-bis(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan

1.2 Other means of identification

Product number -
Other names 3-Methyl-3 H-1,2,3-triazole-4-carboxaldehyde

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:85262-96-0 SDS

85262-96-0Relevant articles and documents

Making Carbonyls of Amides Nucleophilic and Hydroxyls of Alcohols Electrophilic Mediated by SO2F2 for Synthesis of Esters from Amides

Fang, Wan-Yin,Zha, Gao-Feng,Qin, Hua-Li

supporting information, p. 8657 - 8661 (2019/10/17)

We discovered that with the promotion of sulfuryl fluoride, the carbonyl groups of amides performed as nucleophiles while the hydroxyl groups of alcohols were activated to functionalize as electrophiles. This study displayed that the amide C-N bonds could be easily cleaved with delicate nucleophiles to form the ester C-O bonds at room temperature without using transition metals. The broad substrate scope and excellent functional group compatibility were proved with 44 examples in up to 99% yields.

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