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Benzaldehyde, 2-hydroxy-3-(1-methylpropyl)-, oxime is an organic compound with the chemical formula C11H15NO2. It is a derivative of benzaldehyde, featuring a hydroxyl group at the 2-position and a 1-methylpropyl group at the 3-position. The oxime functional group is present, which is formed by the reaction of the carbonyl group with hydroxylamine. Benzaldehyde, 2-hydroxy-3-(1-methylpropyl)-, oxime is known for its unique chemical properties and potential applications in various fields, such as pharmaceuticals and chemical research. It is important to handle Benzaldehyde, 2-hydroxy-3-(1-methylpropyl)-, oxime with care due to its potential reactivity and sensitivity to certain conditions.

155138-08-2

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155138-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155138-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,1,3 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155138-08:
(8*1)+(7*5)+(6*5)+(5*1)+(4*3)+(3*8)+(2*0)+(1*8)=122
122 % 10 = 2
So 155138-08-2 is a valid CAS Registry Number.

155138-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butan-2-yl-6-[(hydroxyamino)methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Benzaldehyde,2-hydroxy-3-(1-methylpropyl)-,oxime

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:155138-08-2 SDS

155138-08-2Downstream Products

155138-08-2Relevant academic research and scientific papers

Magnesium-mediated ortho-Specific Formylation and Formaldoximation of Phenols

Aldred, Robert,Johnston, Robert,Levin, Daniel,Neilan, James

, p. 1823 - 1832 (2007/10/02)

Deprotonation of phenols using magnesium methoxide, followed by distillative removal of free methanol and addition of paraformaldehyde results in ortho-specific magnesium mediated formylation to give the corresponding salicyladehyde magnesium salts, from which the salicylaldehydes can be isolated by acidic work-up.Addition of aq. hydroxylamine sulfate to the salicylaldehyde magnesium salt, in place of the acid work-up, gives the corresponding salicylaldoximes.

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