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7154-01-0

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7154-01-0 Usage

Description

Safrolglycol is a colorless to pale yellow liquid chemical compound known for its floral, sweet, and spicy aroma. It is commonly used in the production of perfumes and fragrances and possesses solvent properties, making it versatile for various industrial applications.

Uses

Used in Perfumery and Fragrance Industry:
Safrolglycol is used as a fragrance ingredient for its distinctive floral, sweet, and spicy scent. It is incorporated into a wide range of personal care products such as soaps, lotions, and cosmetics to provide a pleasant and long-lasting aroma.
Used in Industrial Applications:
Due to its solvent properties, Safrolglycol is utilized in various industrial processes. It can be employed as a solvent in the manufacturing of certain products, helping to dissolve and mix components effectively, thereby enhancing the production process and end-product quality.

Check Digit Verification of cas no

The CAS Registry Mumber 7154-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7154-01:
(6*7)+(5*1)+(4*5)+(3*4)+(2*0)+(1*1)=80
80 % 10 = 0
So 7154-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O4/c11-5-8(12)3-7-1-2-9-10(4-7)14-6-13-9/h1-2,4,8,11-12H,3,5-6H2

7154-01-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1,3-benzodioxol-5-yl)propane-1,2-diol

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:7154-01-0 SDS

7154-01-0Relevant articles and documents

Site-Selective Mono-Oxidation of 1,2-Bis(boronates)

Yan, Lu,Morken, James P.

supporting information, p. 3760 - 3763 (2019/05/24)

Site-selective oxidation of vicinal bis(boronates) is accomplished through the use of trimethylamine N-oxide in 1-butanol solvent. The reaction occurs with good efficiency and selectivity across a range of substrates, providing 2-hydro-1-boronic esters which are shown to be versatile intermediates in the synthesis of chiral building blocks.

LITHIATION OF THE BENZENE RING IN THE PRESENCE OF ortho-ALKYL SUBSTITUENTS BEARING ONE OR TWO HETEROATOMS ON THE β-CARBON. A CONVENIENT SYNTHESIS OF MELLEIN AND KIGELIN

Napolitano, Elio,Morsani, Massimo,Fiaschi, Rita

, p. 249 - 255 (2007/10/02)

The title reaction can be successfully accomplished by proton-metal exchange with n-butyllithium, and the usually observed elimination to a styrene derivative suppressed, provided an appropriate combination of heteroatoms bound to the β-carbon of the alky

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