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1,4-Di-tert-butoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15360-01-7

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15360-01-7 Usage

Physical state

Colorless liquid

Solubility

Insoluble in water

Odor

Strong

Uses

a. Solvent
b. Intermediate in the production of other chemicals
c. Synthesis of pharmaceuticals
d. Synthesis of agrochemicals

Potential applications

a. Flame retardant
b. Lubricant additive

Safety precautions

a. Harmful if inhaled
b. Harmful if swallowed
c. Harmful if skin contact occurs

Check Digit Verification of cas no

The CAS Registry Mumber 15360-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,6 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15360-01:
(7*1)+(6*5)+(5*3)+(4*6)+(3*0)+(2*0)+(1*1)=77
77 % 10 = 7
So 15360-01-7 is a valid CAS Registry Number.

15360-01-7SDS

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 1,4-bis[(2-methylpropan-2-yl)oxy]benzene

1.2 Other means of identification

Product number -
Other names Benzene,p-di-tert-butoxy

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:15360-01-7 SDS

15360-01-7Downstream Products

15360-01-7Relevant academic research and scientific papers

Protection of phenols as t-butyl ethers under mild conditions

Bandgar,Kasture

, p. 252 - 253 (2007/10/03)

Zinc mediated selective O-y-butylation of phenols has been carried out in good to excellent yields under mild conditions. No trace of C-t-butylation was observed.

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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