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p-Nitrocinnamyl chloride, also known as 4-nitrocinnamyl chloride or 4-nitro-β-chlorostyrene, is an organic chemical compound with the molecular formula C9H7ClNO2. It is a yellowish oily liquid that is soluble in organic solvents and has a pungent odor. p-nitrocinnamyl chloride is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. p-Nitrocinnamyl chloride is synthesized through the reaction of 4-nitrocinnamic acid with thionyl chloride or phosphorus trichloride, and it is known for its reactivity in various chemical transformations, such as nucleophilic substitution and elimination reactions. Due to its potential applications in the production of valuable compounds, it is an important building block in the field of organic chemistry.

1507-90-0

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1507-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1507-90-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1507-90:
(6*1)+(5*5)+(4*0)+(3*7)+(2*9)+(1*0)=70
70 % 10 = 0
So 1507-90-0 is a valid CAS Registry Number.

1507-90-0Relevant academic research and scientific papers

NOVEL AROMATIC COMPOUND AND USE THEREOF

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Paragraph 0676-0678, (2016/08/17)

Provided is a compound showing a bone formation promoting action (and/or bone resorption suppressive action). A compound of the formula (I) or a pharmacologically acceptable salt: [wherein each substituent is as defined in the DESCRIPTION], has low toxicity, shows good pharmacokinetics, has an action to promote bone formation, and is useful for the prophylaxis or To treatment of metabolic bone diseases (osteoporosis, fibrous osteitis (hyperparathyroidism), osteomalacia, Paget's disease that influences the systemic bone metabolism parameter etc.) associated with a decrease in the bone formation ability as compared to the bone resorption capacity.

Treatment of alcohols with tosyl chloride does not always lead to the formation of tosylates

Ding, Rui,He, Yong,Wang, Xiao,Xu, Jingli,Chen, Yurong,Feng, Man,Qi, Chuanmin

experimental part, p. 5665 - 5673 (2011/09/20)

Treatment of substituted benzyl alcohols with tosyl chloride resulted in the formation of the corresponding chlorides, not the usual tosylates. A series of experiments demonstrated that it was possible to predict whether chlorination or tosylation would occur for substituted benzyl alcohols and pyridine methanols. Treatment of electron withdrawing group-substituted benzyl alcohols with tosyl chloride gave the corresponding chlorides in moderate yields under mild conditions, which provided a simple way to directly prepare chlorides from alcohols.

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