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3-HYDROXY-3-METHYL-D3-PENTANEDIOIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59060-36-5

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59060-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59060-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,6 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59060-36:
(7*5)+(6*9)+(5*0)+(4*6)+(3*0)+(2*3)+(1*6)=125
125 % 10 = 5
So 59060-36-5 is a valid CAS Registry Number.

59060-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-HYDROXY-3-METHYL-D3-PENTANEDIOIC ACID

1.2 Other means of identification

Product number -
Other names 3-hydroxy-3-<methyl-2H3>pentane-1,5-dioic acid

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:59060-36-5 SDS

59060-36-5Relevant academic research and scientific papers

Biosynthesis of polyketide-terpenoid (Meroterpenoid) metabolites andibenin B and andilesin A in aspergillus variecolor

Simpson, Thomas J.,Anmed, Salman A.,McIntyre, C. Rupert,Scott, Fiona E.,Sadler, Ian H.

, p. 4013 - 4034 (2007/10/03)

Incorporation of 13C-labelled acetates and nethionine indicate that andibenin B (1) and andilesin A (5), C25 metabolites of Aspergillus variecolor, are biosynthesised via a mixed polyketide-terpenoid pathway, 18O-Labelling studies, and incorporation of aromatic precursors and mevalonic acids variously labelled with 13C, 2H and 18O provide evidence for the extensive oxidative and other modifications involved in the elaboration of the highly oxygenated polycyclic structures found in these metabolites. The biosynthetic interrelationships among these and other complex meroterpenoid metabolites are discussed.

Ring D Expansion and Aromatisation in the Biosynthesis of Nic-1, an Antifeedant Steroid from Nicandra physaloides

Gill, Harjit K.,Smith, Roland W.,Whiting, Donald A.

, p. 2989 - 2993 (2007/10/02)

Isotope administration experiments with Nicandra physaloides plants using 2H3>- and 14C3>-mevalonic acid, analysed by 2H NMR and by degradation, respectively, show that the aromatic ring-D of Nic-1 (2) is formed by ring-D expansion in a steroid precursor with oxidative inclusion of the C/D angular methyl.

A Convenient Synthesis of Isotopically Labelled Anthraquinones, Chrysophanol, Islandicin, and Emodin. Incorporation of Chrysophanol into Tajixanthone in Aspergillus variecolor

Ahmed, Salman A.,Bardshiri, Esfandiar,Simpson, Thomas J.

, p. 883 - 884 (2007/10/02)

Cycloaddition reactions of labelled 6-methoxy-3-methyl-2-pyrone (1) with naphthoquinones provide the common fungal anthraquinones, chrysophanol (2), islandicin (3), and emodin (4) suitably labelled for biosynthetic studies, as demonstrated by synthesis and incorporation of chrysophanol into the xanthone metabolite, tajixanthone (17) in Aspergillus variecolor.

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