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88909-06-2

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88909-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88909-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,0 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88909-06:
(7*8)+(6*8)+(5*9)+(4*0)+(3*9)+(2*0)+(1*6)=182
182 % 10 = 2
So 88909-06-2 is a valid CAS Registry Number.

88909-06-2SDS

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 4-(buta-1,3-dienyl)-1,2-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names Z-1-(3,4-dimethoxyphenyl)-1,3-butadiene

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:88909-06-2 SDS

88909-06-2Downstream Products

88909-06-2Relevant articles and documents

Selective 1,2-Aminoisothiocyanation of 1,3-Dienes Under Visible-Light Photoredox Catalysis

Guo, Weisi,Wang, Qian,Zhu, Jieping

supporting information, p. 4085 - 4089 (2020/12/25)

Selective three-component 1,2-diamination of 1,3-dienes with concurrent introduction of two orthogonally protected amino groups remains unknown despite its significant synthetic potential. We report herein that reaction of conjugated dienes with N-aminopy

Aqueous Wittig reactions of semi-stabilized ylides. A straightforward synthesis of 1,3-dienes and 1,3,5-trienes

McNulty, James,Das, Priyabrata

experimental part, p. 5737 - 5740 (2009/12/06)

A direct synthesis of 1,3-dienes and 1,3,5-trienes from the reaction of semi-stabilized ylides and a range of saturated and unsaturated aldehydes is reported in water as solvent, employing sodium hydroxide as base. The water-soluble phosphine oxide side p

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