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21436-26-0

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21436-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21436-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21436-26:
(7*2)+(6*1)+(5*4)+(4*3)+(3*6)+(2*2)+(1*6)=80
80 % 10 = 0
So 21436-26-0 is a valid CAS Registry Number.

21436-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5,5-trimethyl-1-prop-2-enylcyclohex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 1-allyl-3,5,5-trimethyl-2-cyclohexen-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:21436-26-0 SDS

21436-26-0Downstream Products

21436-26-0Relevant articles and documents

Highly Regioselective Allylation of α-Enones and Epoxides with Lithium Tetraallyllanthanoid Ate Complex

Fukuzawa, Shin-ichi,Sakai, Shizuyoshi

, p. 3308 - 3314 (2007/10/02)

Tetraallyllanthanoid ate complex (1), which was readily prepared in situ from tetraallyltin, lanthanoid trichloride, and butyllithium in tetrahydrofuran (THF), reacts smoothly with α-enones (3-11) with a high degree of 1,2-regioselectivity (1,2:1,4 = >99:

Organomanganese (II) reagents XX1: Manganese mediated Barbier and Reformatsky like reactions. An efficient route to homoallylic alcohols and β-acetoxyesters

Cahiez,Chavant

, p. 7373 - 7376 (2007/10/02)

Allylic halides and α-bromoesters react with manganese metal in ethyl acetate; THF can also be used as solvent if a catalytic amount of zinc chloride is added to the reaction mixture. When the reaction is performed in the presence of various aldehydes or

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