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6301-72-0

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6301-72-0 Usage

Chemical compound

1,3-benzodioxol-5-ylmethanediyl diacetate

Psychoactive drug

Yes

Effects

Stimulant and hallucinogenic

Recreational use

Common

Mechanism of action

Increases levels of neurotransmitters (serotonin, dopamine, norepinephrine) in the brain

Resulting feelings

Euphoria, increased energy, enhanced sensory perception

Legal status

Illegal in many countries due to potential for abuse and harmful health effects

Health risks

Increased body temperature, dehydration, potential long-term adverse effects on the brain

Clinical trials

Shown promise in treating psychiatric conditions such as post-traumatic stress disorder (PTSD) and anxiety

Check Digit Verification of cas no

The CAS Registry Mumber 6301-72-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6301-72:
(6*6)+(5*3)+(4*0)+(3*1)+(2*7)+(1*2)=70
70 % 10 = 0
So 6301-72-0 is a valid CAS Registry Number.

6301-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [acetyloxy(1,3-benzodioxol-5-yl)methyl] acetate

1.2 Other means of identification

Product number -
Other names 5-Diacetoxymethyl-benzo[1,3]dioxol

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:6301-72-0 SDS

6301-72-0Downstream Products

6301-72-0Relevant articles and documents

Solvent-free catalytic preparation of 1,1-diacetates using a silica-supported functional ionic liquid as catalyst

Kang, Li Q.,Cai, Yue Q.,Cheng, Lin

, p. 247 - 249 (2013/07/27)

An efficient and convenient preparation of acylals from aldehydes and acetic anhydride, under solvent-free conditions, in the presence of a silica-supported functional ionic liquid, Si-[SbSipim][PF6], is reported. Si-[SbSipim][PF6] acts as a catalyst and can be recovered and reused four times without apparent loss of its catalytic activity.

A convenient and efficient protocol for the synthesis of acylals catalyzed by Br?nsted acidic ionic liquids under ultrasonic irradiation

Borikar, Sanjay P.,Daniel, Thomas

experimental part, p. 928 - 931 (2012/03/08)

The synthesis of acylals (1,1-diacetates) via the reactions of aldehydes with acetic anhydride was carried out in 85-97% yields at room temperature under ultrasound irradiation catalyzed by the Br?nsted acidic ionic liquid [bmpy]HSO4. This method provides several advantages, such as solvent-free conditions, operational simplicity, higher yields, and reduced environmental consequences. The ionic liquid was recovered and reused.

Silica phosphoric acid: An efficient and recyclable catalyst for the solvent-free synthesis of acylals and their deprotection in MeOH

Zhang, Fuyi,Liu, Hong,Zhang, Qing-Ju,Zhao, Yu-Fen,Yang, Feng-Ling

experimental part, p. 3240 - 3250 (2010/12/24)

Silica phosphoric acid was used as an efficient, mild, and recyclable solid catalyst for the synthesis of acylals from various structurally diverse aldehydes and acetic anhydride under solvent-free conditions. The acylation of aldehydes was highly chemoselective, and no ketone was acylated, which provided a method for the synthesis of acylals from aldehydes in the presence of ketones. Silica phosphoric acid-catalyzed deprotection of acylals to the corresponding aldehydes in MeOH has also been developed with excellent yield. The deprotection of the acylals of aromatic aldehydes took priority over those of aliphatic aldehydes. Copyright Taylor & Francis Group, LLC.

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