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5694-99-5

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5694-99-5 Usage

Physical state

Colorless liquid A transparent, colorless liquid without any color.

Odor

Mild, sweet A gentle and pleasant aroma that is slightly sweet in nature.

Primary use

Fragrance ingredient Used mainly as a component in various consumer products to provide a desirable scent.

Derived from

Dioxolane A chemical compound used as a solvent and in the synthesis of other organic compounds.

Potential applications

Pharmaceutical and agricultural industries Possible uses in these fields, but not widely documented.

Safety precautions

Causes irritation or allergic reactions Can lead to skin irritation or allergic reactions in some individuals upon skin contact or inhalation, so it should be handled with care.

Check Digit Verification of cas no

The CAS Registry Mumber 5694-99-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,9 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5694-99:
(6*5)+(5*6)+(4*9)+(3*4)+(2*9)+(1*9)=135
135 % 10 = 5
So 5694-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O3/c1-3-4-5-9(8-11)10(2)12-6-7-13-10/h9,11H,3-8H2,1-2H3

5694-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methyl-1,3-dioxolan-2-yl)hexan-1-ol

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:5694-99-5 SDS

5694-99-5Downstream Products

5694-99-5Relevant articles and documents

Redox-Annulation of Cyclic Amines and β-Ketoaldehydes

Chen, Weijie,Seidel, Daniel

supporting information, p. 1024 - 1027 (2016/03/15)

Benzo[a]quinolizine-2-one derivatives are readily assembled from 1,2,3,4-tetrahydroisoquinoline and β-ketoaldehydes by means of a new intramolecular redox-Mannich process. These reactions are promoted by simple acetic acid and are thought to involve azomethine ylides as reactive intermediates.

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