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132454-41-2

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132454-41-2 Usage

Main properties

1. Chemical compound
2. Complex structure
3. Pyrrolidinedione ring
4. Benzoyl group
5. Chlorine atom
6. Methoxy groups
7. Used in chemical reactions
8. Used in organic synthesis
9. Reactive compound
10. Handle with caution

Specific content

Contains a pyrrolidinedione ring
Contains a benzoyl group attached to the ring
Contains a chlorine atom attached to the benzoyl group
Contains several methoxy groups attached to a phenyl ring
Used in various chemical reactions
Used in organic synthesis processes
Requires caution and adherence to safety protocols due to potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 132454-41-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132454-41:
(8*1)+(7*3)+(6*2)+(5*4)+(4*5)+(3*4)+(2*4)+(1*1)=102
102 % 10 = 2
So 132454-41-2 is a valid CAS Registry Number.

132454-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Succinimidyl-4-<bis-(4-methoxyphenyl)-chloromethyl>-benzoate

1.2 Other means of identification

Product number -
Other names N-succinimidyl-4-[bis(4-methoxyphenyl)chloromethyl]-benzoate

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:132454-41-2 SDS

132454-41-2Downstream Products

132454-41-2Relevant articles and documents

Acid labile immunoconjugate intermediates

-

, (2008/06/13)

Trityl derivatives useful as "linkers" for preparation of imunoconjugates comprising drugs end antibodies are provided. Immunoconjugates and processes for their preparation and use are also provided. This invention also provides for prodrugs comprising a

Heterobifunctional Trityl Derivatives as Linking Reagents for the Recovery of Nucleic Acids after Labeling and Immobilization

Leikauf, Eckart,Barnekow, Frank,Koester, Hubert

, p. 3793 - 3802 (2007/10/02)

The synthesis of two heterobifunctional 4,4'-dimethoxytrityl derivatives carrying a N-hydroxysuccinic acid group as active ester in para 5a or meta position 5b is described.While 5a has been synthesized previously via six steps a novel and more efficient four step synthesis for both compounds is introduced here.The meta compound 5b provides for a more acid labile trityl ether linkage compared to the para derivative 5a.Using these compounds as linking agents biopolymers in particular nucleic acids can easily be recovered after labeling or immobilization by treatment with a mild acid such as 80percent aqueous acetic acid.

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