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Nimbiol is a natural, bio-based chemical compound derived from the neem tree, Azadirachta indica. It is known for its potent insecticidal, fungicidal, and antimicrobial properties, making it a versatile and eco-friendly alternative to synthetic chemicals in various applications. Nimbiol is used in agriculture to control pests and diseases, in pharmaceuticals for its anti-inflammatory and antiseptic effects, and in personal care products for its skin-friendly properties. Its safety and effectiveness have been recognized, contributing to its growing popularity in sustainable and organic product markets.

561-95-5

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561-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 561-95-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 561-95:
(5*5)+(4*6)+(3*1)+(2*9)+(1*5)=75
75 % 10 = 5
So 561-95-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O2/c1-11-8-12-13(9-14(11)19)18(4)7-5-6-17(2,3)16(18)10-15(12)20/h8-9,16,19H,5-7,10H2,1-4H3/t16-,18+/m0/s1

561-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-nimbiol

1.2 Other means of identification

Product number -
Other names 12-hydroxy-13-methyl-podocarpa-8,11,13-trien-7-one

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:561-95-5 SDS

561-95-5Downstream Products

561-95-5Relevant academic research and scientific papers

Highly efficient synthesis of (+)-nimbiol and other podocarpanes derivatives from sclareol

Marcos, Isidro S.,Beneitez, Alvaro,Casta?eda, Lourdes,Moro, Rosalina F.,Basabe, Pilar,Diez, David,Urones, Julio G.

, p. 1589 - 1590 (2008/02/04)

A new access to tricyclic diterpenes of podocarpane skeleton has been opened, in excellent overall yields, and an efficient synthesis of (+)-nimbiol from sclareol has been achieved. Georg Thieme Verlag Stuttgart.

Facile access to optically active ring C aromatic diterpene derivatives from manool. Highly efficient syntheses of (+)-12-methyl-7-oxo-podocarpa-8,11,13-triene-13-carboxylic acid, (+)-13-methyl-7-oxopodocarpa-8,11,13-triene-12-carboxylic acid and (+)-nimbiol

Nakano, Tatsuhiko,Alonso, Randolph,Maillo, Maria Aracelis,Martin, Alfonso,Nunez, Ramona Avila

, p. 1423 - 1426 (2007/10/03)

The extension of our recently developed strategy using the key intermediate 2, obtainable in two steps (52% overall yield) from manool 1, to the synthesis of naturally occurring ring C aromatic diterpene derivatives provides in three steps (+)-12-methyl-7-oxopodocarpa-8,11,13-triene-13-carboxylic acid 4b and its isomer 6b, and in seven steps (+)-nimbiol 11b, in good overall yields. This synthesis discloses that the structure 4b assigned to margolone isolated from Azadirachta indica A. Juss is incorrect and needs to be reinvestigated.

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