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3,5-Dimethoxybenzyl 4-Nitrophenyl Carbonate is a complex organic chemical compound with the molecular formula C16H16N2O7. It is a white crystalline solid that is soluble in organic solvents such as dichloromethane and acetonitrile. 3,5-Dimethoxybenzyl 4-Nitrophenyl Carbonate is primarily used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. It is known for its ability to act as a protecting group in peptide synthesis, where it can be used to temporarily block the reactivity of certain functional groups. The compound is also valued for its stability and ease of removal under mild conditions, which makes it a useful tool in the synthesis of complex molecules. Its structure features a benzyl group with two methoxy substituents at the 3 and 5 positions, and a 4-nitrophenyl group attached to a carbonate moiety, which contributes to its reactivity and utility in chemical reactions.

6453-62-9

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6453-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6453-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6453-62:
(6*6)+(5*4)+(4*5)+(3*3)+(2*6)+(1*2)=99
99 % 10 = 9
So 6453-62-9 is a valid CAS Registry Number.

6453-62-9SDS

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 4-nitrophenyl 3,5-dimethoxybenzyl carbonate

1.2 Other means of identification

Product number -
Other names [3,5-Dimethoxy-benzyl]-p-nitro-phenyl-carbonat

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

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More Details:6453-62-9 SDS

6453-62-9Relevant academic research and scientific papers

External-Radiation-Induced Local Hydroxylation Enables Remote Release of Functional Molecules in Tumors

Duan, Dongban,Fu, Qunfeng,Li, Hongyu,Liu, Zhibo,Ma, Huimin,Shen, Siyong,Wang, Changlun

supporting information, p. 21546 - 21552 (2020/09/07)

Radiation-induced cleavage for controlled release in vivo is yet to be established. We demonstrate the use of 3,5-dihydroxybenzyl carbamate (DHBC) as a masking group that is selectively and efficiently removed by external radiation in vitro and in vivo. D

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