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Benzenemethanol, 4-methoxy-a-(1-methylethenyl)-3-(1-methylethoxy)-2-(1-methyl-1-propen yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

850403-99-5

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850403-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 850403-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,4,0 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 850403-99:
(8*8)+(7*5)+(6*0)+(5*4)+(4*0)+(3*3)+(2*9)+(1*9)=155
155 % 10 = 5
So 850403-99-5 is a valid CAS Registry Number.

850403-99-5SDS

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 1-[3-isopropoxy-4-methoxy-2-(1-methyl-1-propenyl)phenyl]-2-methyl-2-propen-1-ol

1.2 Other means of identification

Product number -
Other names 1-[3-Isopropoxy-4-methoxy-2-((E)-1-methyl-propenyl)-phenyl]-2-methyl-prop-2-en-1-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:850403-99-5 SDS

850403-99-5Downstream Products

850403-99-5Relevant academic research and scientific papers

Ring-closing metathesis for the synthesis of substituted indenols, indenones, indanones and indenes: Tandem RCM-dehydrogenative oxidation and RCM-formal redox isomerization

Coyanis, E. Mabel,Panayides, Jenny-Lee,Fernandes, Manuel A.,de Koning, Charles B.,van Otterlo, Willem A.L.

, p. 5222 - 5239 (2007/10/03)

A number of substituted indenols have been synthesized using ruthenium-mediated ring-closing metathesis (RCM) with Grubbs second generation catalyst as the key step. The required dienes were synthesized by two strategies. The first entailed the isomerizat

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