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10553-38-5

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10553-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10553-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,5 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10553-38:
(7*1)+(6*0)+(5*5)+(4*5)+(3*3)+(2*3)+(1*8)=75
75 % 10 = 5
So 10553-38-5 is a valid CAS Registry Number.

10553-38-5SDS

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 1,1,4,4-tetramethoxycyclohexane

1.2 Other means of identification

Product number -
Other names 1,1,4,4,-tetramethoxycyclohexane

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:10553-38-5 SDS

10553-38-5Downstream Products

10553-38-5Relevant articles and documents

Synthesis of camphoric anhydride via unsensitized photo-oxidation of camphorquinone

Ji, Shun-Jun,Lu, Jianmei,Lang, Jian-Ping,Horiuchi, C. Akira

, p. 1659 - 1663 (2002)

Camphorquinone undergoes a novel unsensitized photo oxidation in polar solvents such as alcohol under oxygen to give camphoric anhydride in 85% yield irradiated with a high-pressure mercury lamp. A possible mechanism is also presented in terms of results of experiment.

High-pressure-promoted uncatalyzed ketalization of ketones and oxy-Michael/ketalization of conjugated enones

Kumamoto, Koji,Ichikawa, Yoshiyasu,Kotsuki, Hiyoshizo

, p. 2254 - 2256 (2007/10/03)

A new practical method for ketalization or oxy-Michael/ketalization was developed using the high-pressure-promoted condensation of ketones or α,β-unsaturated ketones with alcohols in the presence of trialkyl orthoformates as water scavengers. Georg Thieme Verlag Stuttgart.

Ce(3+)-Exchanged Montmorillonite (Ce(3+)-Mont) as a Useful Substrate-Selective Acetalization Catalyst

Tateiwa, Jun-ichi,Horiuchi, Hiroki,Uemura, Sakae

, p. 4039 - 4043 (2007/10/02)

The acetalization of carbonyl compounds with methanol was investigated in the presence of a cation-exchanged montmorillonite (M(n+)-mont; M(n+) = Ce(3+), Zr(4+), Fe(3+), Al(3+), Zn(2+), H(+) and Na(1+).Ce(3+)-mont was found to be the most effective catalyst for substrate-selective acetalization.Cyclohexanones, benzaldehydes, and acid-sensitive 2-furancarboxaldehyde were converted nearly quantitatively to the corresponding acetals in methanol at 25 deg C in the presence of Ce(3+)-mont.The substrates were activated by a Lewis acidic Ce(3+) cation in the interlayer space on the order of 1 kJ mol-1 as measured by FT-IR.The turnover number was estimated to be up to 2.6E3 based on the number of active acid sites in Ce(3+)-mont.

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