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1,3-Cyclohexanedione, 97%, may cont. up to 1% NaCl
1,3-Cyclohexanedione, 97%, may cont. up to 1% NaCl
1,3-Cyclohexanedione, 97%, may cont. up to 1% NaCl
Thermo Scientific Chemicals

1,3-Cyclohexanedione, 97%, may cont. up to 1% NaCl

CAS: 504-02-9 | C6H8O2 | 112.128 g/mol
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数量:
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100 g
1000 g
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製品番号（カタログ番号） A11109.22
または、製品番号A11109-22
価格（JPY）
-
数量:
100 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS504-02-9
IUPAC Namecyclohexane-1,3-dione
Molecular FormulaC6H8O2
InChI KeyHJSLFCCWAKVHIW-UHFFFAOYSA-N
SMILESO=C1CCCC(=O)C1
さらに表示
仕様Specification Sheetスペックシート
Chloride content<1.0% (as sodium chloride)
Melting Point100-105?C
FormPowder or chunks
Appearance (Color)White to cream or pale yellow to pale brown
Assay (Aqueous acid-base Titration)≥96.0 to ≤104.0% (dry weight basis)
さらに表示
It is used as a nitisinone intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used as a nitisinone intermediate.

Solubility
Soluble in water (155 g/L) at 20°C, alcohol, chloroform, acetone, boiling benzene, ether (slightly), carbon disulfide (slightly), and petr ether (slightly).

Notes
Air & Light Sensitive. Store in cool, dry conditions in well sealed containers. Store away from strong oxidizing agents. Keep container tightly closed.
RUO – Research Use Only

General References:

  1. Biswanath Das,; Ponnaboina Thirupathi,; K. Ravinder Reddy,; B. Ravikanth,; Lingaiah Nagarapu.1,3-Cyclohexanedione, 97+%, may cont. up to 1% NaCl. Catalysis Communications.2007 , 8 (3),535-538.
  2. authors. title . Journal name. year of publication , volume issue , pg no.
  3. For procedures for the conversion to the mono- and bis-silyl enol ethers, using HMDS/ imidazole and LDA/ TMS chloride respectively, see: Synthesis, 431 (1977).
  4. Reacts with primary amines to give ß-amino enones, which can be aromatized to m-amino-phenols by oxidation with Hg(OAc)2: Synthesis, 471 (1982).