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7153-33-5

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7153-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7153-33-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7153-33:
(6*7)+(5*1)+(4*5)+(3*3)+(2*3)+(1*3)=85
85 % 10 = 5
So 7153-33-5 is a valid CAS Registry Number.

7153-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[2-oxo-2-[2-[(6-oxocyclohexa-2,4-dien-1-ylidene)methyl]hydrazinyl]ethyl]azanium

1.2 Other means of identification

Product number -
Other names salicylidene Girard-T hydrazone

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:7153-33-5 SDS

7153-33-5Downstream Products

7153-33-5Relevant articles and documents

Enhancing the kinetics of hydrazone exchange processes: An experimental and computational study

Higgs, Patrick L.,Ruiz-Sanchez, Antonio J.,Dalmina, Milene,Horrocks, Benjamin R.,Leach, Andrew G.,Fulton, David A.

supporting information, p. 3218 - 3224 (2019/03/26)

The capacity of hydrazone bonds to readily undergo component exchange processes sees their extensive utilization in dynamic combinatorial chemistry. The kinetics of hydrazone exchange are optimal at pH ~4.5, which limits the use of hydrazone-based dynamic combinatorial libraries, particularly for biological targets which are only stable at near-neutral pH values. It would thus be advantageous if hydrazone exchange proceeded with faster rates at pH values closer to neutral. We experimentally and computationally evaluated the hypothesis that hydrazones possessing neighbouring acidic or basic functional groups within the carbonyl-derived moitety of the hydrazone would enhance exchange rates. Our work suggests that judiciously placed N- or O-hydrogen bond acceptors within the carbonyl-derived moiety of the hydrazone stabilize transition states via hydrogen bonding interactions, providing a valuable boost to exchange kinetics at near-neutral pH values. We anticipate these findings will be of interest in dynamic combinatorial chemistry, dynamic covalent polymers/materials, functionalized nanoparticles and interlocked molecules, all of which may benefit from hydrazone exchange processes able to operate at near-neutral pH values.

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