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122788-52-7

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122788-52-7 Usage

Physical state

Colorless liquid

Uses

a. Production of polymers
b. Production of resins
c. Production of adhesives
d. Solvent
e. Synthesis of other chemical compounds

Boiling point

High boiling point (specific value not provided)

Solubility

Soluble in water

Industrial applications

Useful in various industrial applications due to its properties

Safety

Handle with care and follow proper safety protocols

Health and environmental hazards

Potential health and environmental hazards (specific hazards not provided)

Check Digit Verification of cas no

The CAS Registry Mumber 122788-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,7,8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122788-52:
(8*1)+(7*2)+(6*2)+(5*7)+(4*8)+(3*8)+(2*5)+(1*2)=137
137 % 10 = 7
So 122788-52-7 is a valid CAS Registry Number.

122788-52-7Relevant articles and documents

A novel route to spiro phosphorus-heterocycle via Lawesson's reagent

He, Liangnian,Luo, Yanping,Li, Kai,Ding, Mingwu,Lu, Aihong,Liu, Xiaopeng,Wu, Tianjie,Cai, Fei

, p. 1415 - 1419 (2002)

2-Aryl-spiro-[5,5]-1,3,2-dioxaphosphorinane-2-sufides were prepared by the cyclization reaction of Lawesson's reagent with pentaerythritol and monobenzalpentaerythritol, respectively.

Highly fluorinated metal complexes as dual 19F and PARACEST imaging agents

Yu, Meng,Bouley, Bailey S.,Xie, Da,Que, Emily L.

supporting information, p. 9337 - 9341 (2019/07/04)

We reported a set of water-soluble transition metal complexes that can serve as both 19F and PARACEST magnetic resonance imaging agents. The high number of equivalent fluorine atoms and the paramagnetic effect of metals offer these complexes hi

Mimicking biological membranes with programmable glycan ligands self-assembled from amphiphilic Janus glycodendrimers

Zhang, Shaodong,Moussodia, Ralph-Olivier,Sun, Hao-Jan,Leowanawat, Pawaret,Muncan, Adam,Nusbaum, Christopher D.,Chelling, Kathleen M.,Heiney, Paul A.,Klein, Michael L.,André, Sabine,Roy, René,Gabius, Hans-J.,Percec, Virgil

supporting information, p. 10899 - 10903 (2015/03/30)

An accelerated modular synthesis produced 18 amphiphilic Janus glycodendrimers with three different topologies formed from either two or one carbohydrate head groups or a mixed constellation with a noncarbohydrate hydrophilic arm. By simple injection of their THF solutions into water or buffer, all of the Janus compounds self-assembled into uniform, stable, and soft unilamellar vesicles, denoted glycodendrimersomes. The mixed constellation topology glycodendrimersomes were demonstrated to be most efficient in binding plant, bacterial, and human lectins. This evidence with biomedically relevant receptors offers a promising perspective for the application of such glycodendrimersomes in targeted drug delivery, vaccines, and other areas of nanomedicine.

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