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1-(o-Chlorphenyl)-2-nitro-penten is a chemical compound with the molecular formula C11H12ClNO2. It is an organic compound that features a penten (five-carbon) chain with a nitro group at the second carbon and an o-chlorophenyl group attached to the first carbon. The o-chlorophenyl group refers to a chlorobenzene ring with the chlorine atom attached to the ortho position (adjacent to the point of attachment). 1-(o-Chlorphenyl)-2-nitro-penten is characterized by its yellowish color and is used in the synthesis of various pharmaceuticals and agrochemicals due to its reactive nature and potential to form different functional groups. It is important to handle 1-(o-Chlorphenyl)-2-nitro-penten with care, as it may have potential health and environmental impacts due to its nitro and chlorinated aromatic structures.

1208-51-1

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1208-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1208-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1208-51:
(6*1)+(5*2)+(4*0)+(3*8)+(2*5)+(1*1)=51
51 % 10 = 1
So 1208-51-1 is a valid CAS Registry Number.

1208-51-1Downstream Products

1208-51-1Relevant articles and documents

Structure - Activity studies leading to ( - )1-(Benzofuran-2-yl)-2-propylaminopentane, (( - )BPAP), a highly potent, selective enhancer of the impulse propagation mediated release of catecholamines and serotonin in the brain

Yoneda, Fumio,Moto, Toshiaki,Sakae, Masatoshi,Ohde, Hironori,Knoll, Berta,Miklya, Ildiko,Knoll, Joseph

, p. 1197 - 1212 (2001)

The catecholaminergic and serotoninergic neurons in the brain change their performance according to the physiological need via a catecholaminergic/serotoninergic activity enhancer (CAE/SAE) mechanism. Phenylethylamine (PEA), tyramine and tryptamine are th

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