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100102-73-6

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100102-73-6 Usage

Explanation

Different sources of media describe the Explanation of 100102-73-6 differently. You can refer to the following data:
1. The compound consists of 14 carbon atoms and 18 hydrogen atoms.
2. The carbon atoms are arranged in a closed loop, forming a seven-membered ring.
3. The methyl groups are attached to the 3rd, 4th, 7th, and 7th carbon atoms of the ring.
4. The compound is a liquid and appears colorless when at room temperature.
5. It is used as a starting material to create more complex organic molecules.
6. The compound is utilized as a reagent, particularly in the preparation of other organic compounds.
7. The four methyl groups on the cycloheptatriene ring make this compound particularly useful in the creation of complex organic molecules.

Structure

Cyclic hydrocarbon with a seven-membered ring

Substituents

Four methyl groups

Positions of methyl groups

3, 4, 7, and 7

Physical state

Colorless liquid at room temperature

Applications

Building block in organic synthesis

Use as a reagent

In chemical reactions

Unique feature

Presence of four methyl groups

Check Digit Verification of cas no

The CAS Registry Mumber 100102-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,0 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100102-73:
(8*1)+(7*0)+(6*0)+(5*1)+(4*0)+(3*2)+(2*7)+(1*3)=36
36 % 10 = 6
So 100102-73-6 is a valid CAS Registry Number.

100102-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,7,7-tetramethyl-1,3,5-cycloheptatriene

1.2 Other means of identification

Product number -
Other names 3,4,7,7-tetramethylcyclohepta-1,3,5-triene

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:100102-73-6 SDS

100102-73-6Upstream product

100102-73-6Downstream Products

100102-73-6Relevant articles and documents

TRANSFORMATIONS OF 4-HYDROXYMETHYL-2-CARENE OVER POTASSIUM HYDROXIDE

Manukov, E. N.,Vyglazov, O. G.,Chuiko, V. A.,Shingel', I. A.

, p. 1912 - 1914 (2007/10/02)

The dehydration of 4-hydroxymethyl-2-carene over potassium hydroxide at 250 deg C, which leads to the formation of 4-methyl-3(10),4-caradiene and 3,4,7,7-tetramethyl-1,3,5-cycloheptatriene, was investigated.The dehydration is accompanied by a small degree

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