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10240-16-1

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10240-16-1 Usage

General Description

The chemical "(6R)-8β-(1,3-Benzodioxol-5-yl)-5,6,7,8-tetrahydro-3-methoxy-6,7α-dimethylnaphthalen-2-ol" is a complex organic compound with a long, specific name. It is a naphthalenol derivative with a 1,3-benzodioxole substituent and a methoxy group. The compound has a tetrahydro and dimethyl structure, with specific stereochemistry denoted by the (6R) and 7α descriptors. This chemical has potential applications in various fields, including pharmaceuticals, fragrance, and research, due to its unique structure and properties. However, further research and testing are likely necessary to fully understand and utilize the potential of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 10240-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10240-16:
(7*1)+(6*0)+(5*2)+(4*4)+(3*0)+(2*1)+(1*6)=41
41 % 10 = 1
So 10240-16-1 is a valid CAS Registry Number.

10240-16-1SDS

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 otobaphenol

1.2 Other means of identification

Product number -
Other names (6R,7S,8S)-8-Benzo[1,3]dioxol-5-yl-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydro-naphthalen-2-ol

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:10240-16-1 SDS

10240-16-1Downstream Products

10240-16-1Relevant articles and documents

TANDEM CONJUGATE ADDITION-α-ALKYLATION OF UNSATURATED AMIDES. SYNTHESIS OF 1-ARYLTETRALIN LIGNANS

Mpango, G. B.,Snieckus, V.

, p. 4827 - 4830 (2007/10/02)

The amide alcohols 5,6, obtained in one step from the sequential reaction of N,N-dimethylcrotonamide with dithiane 3 anion and aryl aldehyde 4, were efficiently converted into the lignans galcatin (2a) and isogalcatin (2b).

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