Skip to Content
Merck
All Photos(2)

Key Documents

489492

Sigma-Aldrich

(1S-cis)-3-Bromo-3,5-cyclohexadiene-1,2-diol

0.2 g/mL in 0.1 M phosphate buffer, 96%

Synonym(s):

(1S,2S)-3-Bromo-3,5-cyclohexadiene-1,2-diol

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C6H7BrO2
CAS Number:
Molecular Weight:
191.02
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

optical activity

[α]22/D +20°, c = 1 in methanol

concentration

0.2 g/mL in 0.1 M phosphate buffer

pH

8.5(adjusted to)

mp

90-94 °C (lit.)

functional group

bromo
hydroxyl

storage temp.

−20°C

SMILES string

O[C@H]1C=CC=C(Br)[C@H]1O

InChI

1S/C6H7BrO2/c7-4-2-1-3-5(8)6(4)9/h1-3,5-6,8-9H/t5-,6+/m0/s1

InChI key

KLPGXZKAVBGFGF-NTSWFWBYSA-N

General description

(1S-cis)-3-Bromo-3,5-cyclohexadiene-1,2-diol is a chiral cis-dienediol employed as a key building block for the preparation of varieties of natural products. It can undergo few chemical reactions like cycloadditions, sigmatropic rearrangements, electrophilic additions, and oxidative cleavage.

Physical form

A suspension in phosphate buffer.

Reconstitution

To recover the pure product from the suspension:
(1)Thaw the frozen suspension and filter the solid. (2) Rinse bottle with a few milliliters of base-washed (aqueous Na2CO3) ethyl acetate. (3) Use the rinsing to wash the solid. (4) Collect solid. (5) To further collect more product from the filtrate: extract filtrate with equal volumes of base-washed (aqueous Na2CO3) ethyl acetate (repeat three times). (6) Dry the ethyl acetate extract over MgSO4. (7) Evaporate the solvent - DO NOT HEAT! (8) Combine solids collected from the suspension and the filtrate. Pure crystals should be stored at -78° C. A suspension of the product in phosphate buffer is stable at 0° C.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Enzymatic dihydroxylation of aromatics in enantioselective synthesis: expanding asymmetric methodology
Hudlicky T, et al.
Aldrichimica Acta, 32, 35-62 (1999)
Medium-scale preparation of useful metabolites of aromatic compounds via whole-cell fermentation with recombinant organisms
Endoma MA, et al.
Organic Process Research & Development, 6(4), 525-532 (2002)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service