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90054-95-8

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90054-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90054-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,5 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 90054-95:
(7*9)+(6*0)+(5*0)+(4*5)+(3*4)+(2*9)+(1*5)=118
118 % 10 = 8
So 90054-95-8 is a valid CAS Registry Number.

90054-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethoxy-3-methylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 2,2-dimethoxy-3-methyl-cyclohexanol

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:90054-95-8 SDS

90054-95-8Relevant articles and documents

α-Hydroxylation on Ketones Using o-Iodosylbenzoic Acid

Moriarty, Robert M.,Hou, Kwang-Chung

, p. 691 - 694 (1984)

o-Iodosylbenzoic acid (KOH/CH3OH) converts various ketones to α-hydroxydimethylacetals in high yield with the advantageous feature of solubility of the reduction product o-iodobenzoic acid under the basic reaction conditions thus allowing isolation of the oxidation product by simple CH2Cl2 extraction.

Indirect electrochemical oxidation of cyclic ketones: Strong influence of ring size on the result of the reaction

Barba, Fructuoso,Elinson, Michail N.,Escudero, Jose,Feducovich, Sergey K.

, p. 5759 - 5762 (2007/10/03)

The result of the indirect electrochemical oxidation of cyclic ketones in methanol in the undivided cell in the presence of sodium iodide depends on the ring size. Cyclopentanone affords 2,2-dimethoxycyclopentanone. While cyclohexanone gives rise 2,2-dimethoxycyclo-hexanol, and cyclic ketones with higher ring size undergo new type of the electrochemically induced Favorskii rearrangement with the formation of methyl cycloalkencarboxylates containing in the ring on the one carbon atom less than starting ketone. So the simple electrocatalytic system can distinguish the ring size of cyclic ketones.

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