Cas 52385-31-6,(S,S,S)-Tris(1-hydroxy-1-methylpropyl)benzol

52385-31-6

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Basic information

Product Name: (S,S,S)-Tris(1-hydroxy-1-methylpropyl)benzol
Synonyms:
CAS NO:52385-31-6
Molecular Formula:
Molecular Weight: 294.434
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S,S,S)-Tris(1-hydroxy-1-methylpropyl)benzol(CAS DataBase Reference)
NIST Chemistry Reference: (S,S,S)-Tris(1-hydroxy-1-methylpropyl)benzol(52385-31-6)
EPA Substance Registry System: (S,S,S)-Tris(1-hydroxy-1-methylpropyl)benzol(52385-31-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 52385-31-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 52385-31-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,8 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52385-31:
(7*5)+(6*2)+(5*3)+(4*8)+(3*5)+(2*3)+(1*1)=116
116 % 10 = 6
So 52385-31-6 is a valid CAS Registry Number.

52385-31-6Upstream product

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52385-31-6Relevant academic research and scientific papers

COTRIMERIZATION REACTIONS OF ACETYLENIC ALCOHOLS IN THE PRESENCE OF BISPHOSPHINE NICKEL COMPLEXES. X-RAY MOLECULAR STRUCTURE OF 1,3,5-TRIS(1-HYDROXY-1-METYLETHYL)BENZENE (1,3,5-TIMEB) AND OF THE ADDUCT OF 1,3,5-TIMEB WITH 2,5-DIMETHYLHEX-3-YN-2,5-DIOL

Furlani, Anita,Hornemann, Karl Heinz,Russo, Maria Vittoria,Villa, Angiola Chiesi,Guastini, Carlo

, p. 429 - 436 (2007/10/02)

The catalytic cyclotrimerization reactions of 2-methylbut-3-yn-2-ol (Mb), 3-methylpent-4-yn-3-ol (Mp),1-ethynylcyclohexane-1-ol (Ec) and 2,5-dimethylhex-3-yn-2,5-diol (DMED) have been studied in the presence of and .The cyclic cotrimers of Mb-Mp, Mb-Ec and the adduct of 1,3,5-tris(1-hydroxy-1-methylethyl)benzene (TIMEB) with DMED have been characterized.The molecular structures of the adduct TIMEB-DMED and of TIMEB have been determined by X-ray crystallography; TIMEB-DMED: monoclinic, a=16.999(3), b=8.907(1), c=32.142(4) Angstroem, z=8, space group C2/c.Each TIMEB molecule is linked to adjacent TIMEB and DMED molecules to originate on one side centrosymmetric tetramers and on the other side tetramers having 21 symmetry.TIMEB: monoclinic, a=28.001(4), b=5.989(1), c=17.127(3) Angstroem, z=8, space group P21/c.A network of H...O hydrogen bonds links together the molecules of TIMEB.

Synthesis of Benzene Derivatives with Several Homochirally-analogous Substituents

Schoenfelder, Wolfgang,Snatzke, Guenther

, p. 1855 - 1866 (2007/10/02)

By cyclotrimerization of the corresponding acetylene derivatives some 1,3,5-trisubstituted benzene derivatives (2a - c, 8a, d) containing three identical chiral groups have been synthesized.The analogous mono- and 1,4-disubstituted products (6, 7) have be

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