1. Home
  2. 1,2-Cyclohexanediol, (1R,2R)-rel-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,2-Cyclohexanediol, (1R,2R)-rel-

O[C@@H]1CCCC[C@H]1O Request for Quotation
Chemical Name: 1,2-Cyclohexanediol, (1R,2R)-rel-
CAS Number: 1460-57-7
Product Number: AG001DLO(AGN-PC-0PY4S6)
Synonyms:
MDL No:
Molecular Formula: C6H12O2
Molecular Weight: 116.1583

Identification/Properties

Computed Properties
Molecular Weight:
116.16g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
116.084g/mol
Monoisotopic Mass:
116.084g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
62.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


trans-Cyclohexane-1,2-diol, also known as trans-1,2-Cyclohexanediol, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the production of various pharmaceuticals, fragrances, and agrochemicals. Its unique structure, consisting of a cyclohexane ring with two hydroxyl groups in trans configuration, imparts specific chemical properties that make it valuable in organic synthesis.In chemical synthesis, trans-Cyclohexane-1,2-diol is commonly employed as a precursor for the synthesis of complex molecules. Its hydroxyl groups can undergo various functionalization reactions, such as esterification, etherification, and oxidation, to introduce different functional groups onto the cyclohexane ring. These modifications enable the creation of structurally diverse compounds with a wide range of applications.trans-Cyclohexane-1,2-diol is particularly useful in the preparation of chiral compounds due to its inherently chiral structure. By utilizing this compound as a starting material, chemists can access enantiomerically pure molecules, crucial in the pharmaceutical industry for the development of new drugs with improved therapeutic properties. Its ability to participate in stereoselective reactions makes it a valuable tool for controlling the stereochemistry of the final product.Overall, trans-Cyclohexane-1,2-diol plays a vital role in chemical synthesis as a versatile and indispensable building block for the construction of complex organic molecules. Its applications extend across various industries, highlighting its significance in modern synthetic chemistry practices.