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103447-97-8

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103447-97-8 Usage

Physical state

Clear, colorless liquid

Odor

Mild

Classification

Glycol ether

Boiling point

High

Volatility

Low

Industrial applications

Solvent in paints, coatings, inks, cleaning products, adhesives, and electronic materials

Toxicity

Relatively non-toxic

Skin contact

Not known to cause harmful effects

Inhalation

Not known to cause harmful effects

Eye irritation

Potential for irritation

Respiratory system

Potential for irritation

Check Digit Verification of cas no

The CAS Registry Mumber 103447-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,4 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103447-97:
(8*1)+(7*0)+(6*3)+(5*4)+(4*4)+(3*7)+(2*9)+(1*7)=108
108 % 10 = 8
So 103447-97-8 is a valid CAS Registry Number.

103447-97-8SDS

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 (+/-)-1-O-(2-methoxyethyl)propane-1,2-diol

1.2 Other means of identification

Product number -
Other names 2,5-dioxaoctan-7-ol

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:103447-97-8 SDS

103447-97-8Downstream Products

103447-97-8Relevant articles and documents

Enhanced reactivity of secondary hydroxyl groups in the O-alkylation of carbohydrate-related primary-secondary vic-glycols. Regioselective 2-O-benzylation of 1,3:2,4-di-O-ethylidene-D-glucitol

El'perina, E. A.,Struchkova, M. I.,Serkebaev, M. I.,Serebryakov, E. P.

, p. 744 - 750 (2007/10/02)

Partial O-alkylation of 1,3:2,4-di-O-ethylidene-D-glucitol (1a), 1,2-O-isopropylidene-3-O-methyl-α-D-glucofuranose (1b), and R-(+)-1-O-benzylglycerol (1c) with benzyl chloride in a KOH/DMSO system results in products of monoalkylation at the secondary (4a-c) and at the primary hydroxyl (2a-c) in ratios of over 95:5 (a), ca. 2:1 (b), and ca. 1:1 (c), whereas (+/-)propane-1,2-diol (1d) gives only the product of 1-O-benzylation (2d).A qualitatively similar result is observed upon O-alkylation of diols (1a-e) with 2-methoxyethanol tosylate.

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