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1698-98-2

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1698-98-2 Usage

Physical state

Colorless to pale yellow liquid

Odor

Faint aromatic

Uses

a. Fragrance ingredient in perfumes
b. Solvent in various industrial applications
c. Viscosity-reducing agent in certain formulations
d. Potential fuel additive for improved combustion performance in internal combustion engines

Limitations

Low flash point and flammability

Versatility

Practical applications in fragrance, solvent, and fuel industries

Check Digit Verification of cas no

The CAS Registry Mumber 1698-98-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1698-98:
(6*1)+(5*6)+(4*9)+(3*8)+(2*9)+(1*8)=122
122 % 10 = 2
So 1698-98-2 is a valid CAS Registry Number.

1698-98-2SDS

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 1,2-di(propan-2-yloxy)benzene

1.2 Other means of identification

Product number -
Other names catechol diisopropyl ether

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:1698-98-2 SDS

1698-98-2Relevant articles and documents

Synthesis of bulky 1,2-dialkoxy- and 1,2,3-trialkoxy-arenes

Stephan, Michel,Zupancic, Borut,Mohar, Barbara

experimental part, p. 6308 - 6315 (2011/09/19)

A large series of bulky 1,2-dialkoxy- and 1,2,3-trialkoxy-benzenes was efficiently prepared via Williamson etherification. Preparation of their contiguous bromine-containing derivatives was also achieved.

A SIMPLE SYNTHESIS OF O-ISOPROPOXYPHENOL

Deodhar, V. B.,Dalavoy, V. S.,Nayak, U. R.

, p. 753 - 754 (2007/10/03)

-

PHOSPHORORGANISCHE VERBINDUNGEN 101. TERTIAERE PHOSPHINE MIT ORTHOALKOXYPHENYL-GRUPPEN. Synthese und Eigenschaften

Horner, L.,Simons, G.

, p. 189 - 210 (2007/10/02)

Alkylphenylethers, ortho-lithiated in good yields, are transformed according to scheme (1) to the triarylphosphines ArPPh2, Ar2PPh and Ar3P (Ar contains in all cases an ortho-alkoxy group) (Table 1.).Hydroquinonedialkylethers can be lithiated twice, forming the compounds 102 and 103.Table 2 summarizes some arylalkylethers (71 - 101) which were lithiated; table 7 presents 12 new arylalkylethers.The syntheses of triarylphosphines with one or two bulky groups (105 - 110) and of triarylphosphines with one or two 3,4-dialkoxyphenyl groups (111 - 114) are reported.The 31P-spectra of the compounds prepared are discussed with respect to the validity of the Tolman-rule.

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