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Methyl 2-hydroxy-6-methyl-3-(propan-2-yl)benzoate is a complex organic chemical compound with the molecular formula C12H16O3. It is a derivative of benzoic acid, featuring a methyl group at the 2-position, a hydroxyl group at the 2-position, a methyl group at the 6-position, and a propyl group at the 3-position. methyl 2-hydroxy-6-methyl-3-(propan-2-yl)benzoate is characterized by its aromatic ring structure, which contributes to its chemical properties and potential applications. It is often used in the synthesis of various pharmaceuticals, fragrances, and other specialty chemicals due to its unique functional groups and structural features.

6547-90-6

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6547-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6547-90-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6547-90:
(6*6)+(5*5)+(4*4)+(3*7)+(2*9)+(1*0)=116
116 % 10 = 6
So 6547-90-6 is a valid CAS Registry Number.

6547-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-hydroxy-6-methyl-3-propan-2-ylbenzoate

1.2 Other means of identification

Product number -
Other names Methyl 2-hydroxy-3-isopropyl-6-methylbenzoate

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 -
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More Details:6547-90-6 SDS

6547-90-6Relevant academic research and scientific papers

Conformational Behaviour of Medium-sized Rings. Part 10. Dithiosalicylides and Trithiosalicylides

Guise, G. Bruce,Ollis, W. David,Peacock, Judith A.,Stephanatou, Julia Stephanidou,Stoddart, J. Fraser

, p. 1637 - 1648 (2007/10/02)

The trithiosalicylide derivatives (8)-(11) have been synthesised and shown by temperature-dependent 1H n.m.r. spectroscopy to exist in solution as ring inverting (35a)(35b) enantiomeric helical conformations with trans-thioester linkages.The free energies of activation for these conformational changes are ca. 10 kcal mol-1 higher than those for the similar process in the corresponding trisalicylides.In contrast with the trisalicylides, the trithiosalicylides can only ring invert between enantiomeric helical conformations via intermediates containing a cis-thioester linkage.The dithiosalicylide derivatives (3)-(7) have been synthesised; the temperature dependence of the 1H n.m.r. spectrum of di-o-thiothymotide (7) has been interpreted in terms of ring inversion (40a)(40b) between enantiomeric boat conformations.Comparison of the ΔG value of 24.6 kcal mol-1 for this conformational change with that of 17.7 kcal mol-1 previously obtained for di-o-thymotide (41) suggests that cis-thioester linkages are subject to more resonance stabilisation than are cis-ester linkages.

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