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The chemical compound "(1S,αS,4aα)-α-Ethenyldecahydro-5α-(hydroxymethyl)-α,5,8aβ-trimethyl-2-methylenenaphthalene-1β-(1-propanol)" is a complex organic molecule with a unique structure. It features a decalin ring system with a naphthalene core, which is further modified by the presence of a vinyl group (α-ethenyl), a hydroxymethyl group (-CH2OH), and a methyl group (-CH3) at specific positions. The compound also includes a propanol side chain attached to the naphthalene ring. This molecule is characterized by its stereochemistry, with the 1S, αS, and 4aα configurations indicating the specific three-dimensional arrangement of atoms around the asymmetric carbon centers. The compound's structure and properties make it a potential candidate for various applications in the fields of chemistry and materials science, such as in the synthesis of pharmaceuticals or as a precursor in the production of specialty chemicals.

4549-12-6

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4549-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4549-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4549-12:
(6*4)+(5*5)+(4*4)+(3*9)+(2*1)+(1*2)=96
96 % 10 = 6
So 4549-12-6 is a valid CAS Registry Number.

4549-12-6Upstream product

4549-12-6Downstream Products

4549-12-6Relevant academic research and scientific papers

Microbial Transformation of Manool and (12Z)-Labda-8(17),12,14-triene by Rhodococcus erythropolis JTS-131

Hieda, Tadaharu,Mikami, Yoichi,Obi, Yukiteru

, p. 787 - 794 (2007/10/02)

Rhodococcus erythropolis JTS-131, a cis-abienol and sclareol transformable bacterium, converted manool and accumulated manoyl oxide in the culture broth.In the presence of metabolic inhibitors, 13β-hydroxylabda-8(17),14-dien-18-oic acid and its methylester (a new compound) were accumulated as the transformation products.This strain also transformed (12Z)-labda-8(17),12,14-triene and accumulated (12Z)-labda-8(17),12,14-trien-18-al in the culture broth.In the presence of metabolic inhibitors, two compounds, (12Z)-labda-8(17),12,14-trien-18-ol and 4,18,19-trinor-3,4-seco-5-oxo-(12Z)-labda-8(17),12,14-trien-3-oic acid were accumulated.Based on the experiments on the degradation sequence, transformation pathways for these two labdanes by the bacterium are proposed.

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