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60102-29-6

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60102-29-6 Usage

General Description

The chemical "2-[(R)-3,4-Dihydro-7-methoxy-2H-1-benzopyran-3-yl]-5-methoxyphenol" refers to a specific organic compound. The structure of the chemical is characterized by the presence of a benzopyran ring system and methoxyphenol, with methoxy groups attached, which are ethers with one of the hydrogens replaced by a methoxy group. The complexity of the name signifies a complex molecular structure. Specific details regarding this chemical's properties such as its molar mass, solubility, reactivity, and detailed uses are not commonly available. As an organic compound, it can potentially be involved in various chemical reactions and could possibly be used in pharmaceuticals, though this would need to be supported by detailed research and data.

Check Digit Verification of cas no

The CAS Registry Mumber 60102-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60102-29:
(7*6)+(6*0)+(5*1)+(4*0)+(3*2)+(2*2)+(1*9)=66
66 % 10 = 6
So 60102-29-6 is a valid CAS Registry Number.

60102-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methoxy-2-[(3R)-7-methoxy-3,4-dihydro-2H-chromen-3-yl]phenol

1.2 Other means of identification

Product number -
Other names JDTic dihydrochloride

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:60102-29-6 SDS

60102-29-6Relevant articles and documents

A general asymmetric route to enantio-enriched isoflavanes via an organocatalytic annulation of o-quinone methides and aldehydes

Zhang, Jian,Zhang, Shuangzhan,Yang, Huixin,Zhou, Ding,Yu, Xueting,Wang, Wei,Xie, Hexin

supporting information, p. 2407 - 2411 (2018/05/24)

Reported herein is a general approach to optically active isoflavanes based on a chiral amine-catalyzed [4 + 2] asymmetric annulation of o-quinone methides and aldehydes. A number of naturally occurring isoflavanes, including equol, sativan, isosativan, v

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