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1,3-Benzodioxol-5-yl dimethylcarbamate is a chemical compound with the molecular formula C10H11NO4. It is a derivative of 1,3-benzodioxole, which is a heterocyclic aromatic compound consisting of a benzene ring fused to a dioxole ring. The dimethylcarbamate functional group is attached to the 5-position of the benzodioxole ring, where two methyl groups are connected to the carbamate group. 1,3-benzodioxol-5-yl dimethylcarbamate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. It is important to note that handling and disposal of this chemical should be done with caution, as it may have toxic properties and require proper safety measures.

2594-29-8

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2594-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2594-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2594-29:
(6*2)+(5*5)+(4*9)+(3*4)+(2*2)+(1*9)=98
98 % 10 = 8
So 2594-29-8 is a valid CAS Registry Number.

2594-29-8Downstream Products

2594-29-8Relevant academic research and scientific papers

Room-temperature Pd-catalyzed C-H chlorination by weak coordination: One-pot synthesis of 2-chlorophenols with excellent regioselectivity

Sun, Xiuyun,Sun, Yonghui,Zhang, Chao,Rao, Yu

supporting information, p. 1262 - 1264 (2014/02/14)

A room-temperature Pd(ii)-catalyzed regioselective chlorination reaction has been developed for a facile one-pot synthesis of a broad range of 2-chlorophenols. The reaction demonstrates an excellent regioselectivity and reactivity for C-H chlorination. This reaction represents one of the rare examples of mild C-H functionalization at ambient temperature.

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