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122948-45-2

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122948-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122948-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122948-45:
(8*1)+(7*2)+(6*2)+(5*9)+(4*4)+(3*8)+(2*4)+(1*5)=132
132 % 10 = 2
So 122948-45-2 is a valid CAS Registry Number.

122948-45-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,3-dimethoxybutyl)-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names 4-(p-Methoxyphenyl)-2-butanone dimethyl acetal

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:122948-45-2 SDS

122948-45-2Relevant articles and documents

Design, synthesis, and structure of alkyl 1H-pyrazolecarboxylates from a raspberry ketone methyl ether

Campos, Patrick T.,Cargnelutti, Roberta,Flores, Alex F. C.,Goulart, Taís B.,Moura, Sidnei,Neves, Adriana M.,Soares, Mayara S. P.,Stefanello, Francieli M.

, p. 1314 - 1320 (2020)

[Figure not available: see fulltext.] This paper reports a one-pot synthesis of 5-[2-(4-methoxyphenyl)ethyl]-1H-pyrazole-3-carboxylates via cyclocondensation of 1,1,1-trichloro-4-methoxy-6-(4-methoxyphenyl)hex-3-en-2-one with hydrazine hydrochloride in RO

An efficient protection of carbonyls and deprotection of acetals using decaborane

Lee, Seung Hwan,Lee, Ji Hee,Yoon, Cheol Min

, p. 2699 - 2703 (2015/10/07)

Carbonyls were efficiently converted to the corresponding dimethyl acetals at room temperature using trimethyl orthoformate and 1 mol% of decaborane under a nitrogen atmosphere. In turn, acetals were deprotected to the corresponding carbonyls using 1 mol% of decaborane in aqueous THF chemoselectively.

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