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34454-77-8

34454-77-8

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34454-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34454-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,5 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34454-77:
(7*3)+(6*4)+(5*4)+(4*5)+(3*4)+(2*7)+(1*7)=118
118 % 10 = 8
So 34454-77-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H18O/c1-6-10(4,5)11-8-7-9(2)3/h6-7H,1,8H2,2-5H3

34454-77-8SDS

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 3-methyl-1-(2-methylbut-3-en-2-yloxy)but-2-ene

1.2 Other means of identification

Product number -
Other names EINECS 252-042-6

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:34454-77-8 SDS

34454-77-8Relevant articles and documents

3-methyl-2-butene-1-aldehyde diisopentenyl acetal

-

Paragraph 0030-0045, (2021/11/06)

The invention relates to 3-methyl-2-butene-1-aldehyde diisopentenyl acetal, which comprises 3-methyl-3-(3-methyl-2-butene-1-oxygen)-1-butene with the mass content of less than 450mg/kg. The prepared 3-methyl-2-butene-1-aldehyde diisopentenyl acetal is high in storage safety and good in stability.

ORGANOTINS AS ETHERIFICATION CATALYSTS. III. ETHERIFICATIONS AND HYDRO-HYDROXY-ELIMINATIONS PROMOTED BY BUTYLTIN TRICHLORIDE

Marton, Daniele,Slaviero, Pierangelo,Tagliavini, Giuseppe

, p. 7099 - 7108 (2007/10/02)

Butyltin trichloride, as a catalyst precursor, promotes the following processes: (i) etherification of 2,3-unsaturated alcohols, (ii) etherification of functional diols, (iii) cyclization of 2,5-hexanedione, and (iv) dehydration of cyclic diols.Many examples are reported.

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