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Cyclohexane, 1-(1,1-dimethylethyl)-4-propoxy-, cis- is a complex organic compound with the molecular formula C12H24O. It is a cyclic alkane with a six-carbon ring structure, where one of the carbon atoms is substituted with a 1,1-dimethylethyl (tert-butyl) group and another carbon atom is substituted with a propoxy group. The cis- configuration indicates that the propoxy group and the tert-butyl group are on the same side of the cyclohexane ring. Cyclohexane, 1-(1,1-dimethylethyl)-4-propoxy-, cis- is known for its unique stereochemistry and is used in various chemical applications, such as a solvent or a precursor in the synthesis of other organic compounds.

1900-60-3

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1900-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1900-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1900-60:
(6*1)+(5*9)+(4*0)+(3*0)+(2*6)+(1*0)=63
63 % 10 = 3
So 1900-60-3 is a valid CAS Registry Number.

1900-60-3SDS

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-tert-butyl-4-propoxycyclohexane

1.2 Other means of identification

Product number -
Other names cis-4-tert-Butyl-1-propoxycyclohexan

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:1900-60-3 SDS

1900-60-3Downstream Products

1900-60-3Relevant academic research and scientific papers

A Novel Entry into Wittig Rearrangements - A Stereoselective -Wittig Rearrangement with Inversion of Configuration at the Carbanion Center

Hoffmann, Rolf,Brueckner, Reinhard

, p. 1957 - 1964 (2007/10/02)

The O,Se ketal 10, through lithium naphthalenide induced reductive cleavage of its Csp3-Se bond, was converted into the α-lithio ether 11a with an equatorially oriented C-O bond.At -78 deg C, 11a undergoes a rapid -Wittig rearra

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