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1,5-Hexanedione, 2-nitro-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88072-88-2

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88072-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88072-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,7 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88072-88:
(7*8)+(6*8)+(5*0)+(4*7)+(3*2)+(2*8)+(1*8)=162
162 % 10 = 2
So 88072-88-2 is a valid CAS Registry Number.

88072-88-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-1-phenylhexane-1,5-dione

1.2 Other means of identification

Product number -
Other names 1,5-Hexanedione,2-nitro-1-phenyl

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:88072-88-2 SDS

88072-88-2Downstream Products

88072-88-2Relevant academic research and scientific papers

Synergistic Noncovalent Catalysis Facilitates Base-Free Michael Addition

Duarte, Fernanda,Lusby, Paul J.,Wang, Jianzhu,Young, Tom A.

, p. 17743 - 17750 (2020)

Carbon-carbon bond-forming processes that involve the deprotonation of a weakly acidic C-H pro-nucleophile using a strong Br?nsted base are central to synthetic methodology. Enzymes also catalyze C-C bond formation from weakly C-H acidic substrates; howev

A New Synthesis of 1,5-Dicarbonyl Compounds under Neutral Conditions

Ono, Noboru,Miyake, Hideyoshi,Kaji, Aritsune

, p. 875 - 876 (2007/10/02)

Michael addition of α-nitroketones to methyl vinyl ketone or acrylaldehyde followed by denitration with Bu3SnH affords 1,5-dicarbonyl compounds in good yields.

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