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39887-30-4

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39887-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39887-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,8 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39887-30:
(7*3)+(6*9)+(5*8)+(4*8)+(3*7)+(2*3)+(1*0)=174
174 % 10 = 4
So 39887-30-4 is a valid CAS Registry Number.

39887-30-4Relevant articles and documents

CRF RECEPTOR ANTAGONISTS AND METHODS OF USE

-

, (2021/06/11)

Compounds are provided herein that antagonize corticotropin-releasing factor (CRF) receptors, in particular CRF receptor 1 (CRF1), as well as related preparations, compositions and methods for treating diseases and/or disorders that would benefit from the same such as congenital adrenal hyperplasia (CAH).

Highly Ag+ selective tripodal Gold(I) acetylide-based "off-On" luminescence chemosensors based on 3(ππ*) emission switching

Zhou, Yu-Peng,Liu, En-Bao,Wang, Jin,Chao, Hsiu-Yi

, p. 8629 - 8637 (2013/09/02)

Newly prepared gold(I) acetylide-based luminescent cation sensors 1c and 1d, which bear a novel three-armed flexible conformation, together with control molecule 2c, were synthesized in four steps. 1c and 1d exhibit the π → π* absorption of the acetylide

A new strategy for preparing molecular imaging and therapy agents using fluorine-rich (fluorous) soluble supports

Donovan, Amanda,Forbes, Jane,Dorff, Peter,Schaffer, Paul,Babich, John,Valliant, John F.

, p. 3536 - 3537 (2007/10/03)

A convenient new strategy for producing radiolabeled compounds in high effective specific activity was developed using soluble fluorous supports. The reported methodology involves a fluorous linker group that is released from the substrate of interest upon reaction with radioiodine. The desired product can then be selectively separated from unreacted starting material and reaction byproducts using a simple fluorous solid-phase extraction procedure. The utility of this approach was demonstrated by labeling a series of benzoic acid derivatives which are commonly used to prepare molecular imaging agents. All compounds were produced in high radiochemical yields, purities, and effective specific activities. The strategy was further elaborated in that it was used to prepare a small collection of radiolabeled benzamides as a way of demonstrating the potential utility of this method for creating libraries of molecular imaging agents. Copyright

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