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10008-88-5

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10008-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10008-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,0 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10008-88:
(7*1)+(6*0)+(5*0)+(4*0)+(3*8)+(2*8)+(1*8)=55
55 % 10 = 5
So 10008-88-5 is a valid CAS Registry Number.

10008-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylaminomethyl)-4-[2-[3-(diethylaminomethyl)-4-hydroxyphenyl]propan-2-yl]phenol

1.2 Other means of identification

Product number -
Other names 2.2-Bis-<4-hydroxy-x-diaethylaminomethyl-phenyl>-propan

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:10008-88-5 SDS

10008-88-5Downstream Products

10008-88-5Relevant articles and documents

Dibromomethane as one-carbon source in organic synthesis: The Mannich base formation from the reaction of phenolic compounds with a preheated mixture of dibromomethane and diethylamine

Hon, Yung-Son,Chou, Yu-Yu,Wu, I-Che

, p. 2253 - 2267 (2007/10/03)

The salt formed from the reaction of dihalomomethane and diethylamine reacted with phenolic compounds to give the corresponding Mannich bases in modest to good yields. As for the relative rates and yields are in the following order: CH2Br2 > CH2Cl2. The CD2Cl2 is also applicable to prepare the deuterated analogues. At higher temperature, the elimination of diethylamine from Mannich base occurred to give the corresponding o-quinone methide intermediate, which was then trapped by another phenolic compound to give bis(2-hydroxy-1-aryl) methanes.

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