S-Boc-2-mercapto-4,6-dimethylpyrimidine

• CAS: 41840-28-2
• Catalog Number: ACM41840282
• Category: tert-Butoxycarbonylation (Boc) Reagents
• Molecular Weight: 240.32
• Molecular Formula: C11H16N2O2S
• Synonyms: O-tert-Butyl-S-(4,6-dimethyl-2-pyrimidinyl) thiocarbonate, Boc-S
• Melting Point: 48-51 °C (lit.)
• Physical State: Powder

Custom Q&A

What is the molecular formula of S-Boc-2-mercapto-4,6-dimethylpyrimidine?

The molecular formula is C11H16N2O2S.

What are some synonyms of S-Boc-2-mercapto-4,6-dimethylpyrimidine?

Some synonyms include 41840-28-2, O-tert-Butyl S-(4,6-dimethylpyrimidin-2-yl) carbonothioate, and tert-butyl (4,6-dimethylpyrimidin-2-yl)sulfanylformate.

When was S-Boc-2-mercapto-4,6-dimethylpyrimidine created and last modified in PubChem?

It was created on 2005-03-27 and last modified on 2023-12-30.

What is the IUPAC name of S-Boc-2-mercapto-4,6-dimethylpyrimidine?

The IUPAC name is tert-butyl (4,6-dimethylpyrimidin-2-yl)sulfanylformate.

What is the InChIKey of S-Boc-2-mercapto-4,6-dimethylpyrimidine?

The InChIKey is POTDIELOEHTPJN-UHFFFAOYSA-N.

What is the molecular weight of S-Boc-2-mercapto-4,6-dimethylpyrimidine?

The molecular weight is 240.32 g/mol.

What is the CAS number of S-Boc-2-mercapto-4,6-dimethylpyrimidine?

The CAS number is 41840-28-2.

What is the XLogP3-AA value of S-Boc-2-mercapto-4,6-dimethylpyrimidine?

The XLogP3-AA value is 3.

How many hydrogen bond acceptors does S-Boc-2-mercapto-4,6-dimethylpyrimidine have?

It has 5 hydrogen bond acceptors.

Is the compound canonicalized in PubChem?

Yes, the compound is canonicalized in PubChem.

Synthetic Use

Downstream Synthesis Route 1

• 39994-75-7
• 41840-28-2

• 60538-19-4
• 22325-27-5

Reference: [1] Chemical and Pharmaceutical Bulletin, 1985, vol. 33, # 4, p. 1342 - 1350

Downstream Synthesis Route 2

• 41840-28-2
• 61478-25-9

• 37813-30-2

Reference: [1] Journal of Organic Chemistry, 1980, vol. 45, # 23, p. 4728 - 4739

Downstream Synthesis Route 3

• 41840-28-2
• 660-88-8

• 27219-07-4

Reference: [1] Carbohydrate Research, 1989, vol. 194, # C, p. 199 - 208

Downstream Synthesis Route 4

• 107-10-8
• 41840-28-2

• 105678-25-9

Reference: [1]Tanaka, Ken-Ichi; Yoshifuji, Shigeyuki; Nitta, Yoshihiro
[Chemical and pharmaceutical bulletin, 1988, vol. 36, # 8, p. 3125 - 3129]

Downstream Synthesis Route 5

• 14753-26-5
• 41840-28-2

• 116861-31-5

Reference: [1]Chemical and pharmaceutical bulletin,1988,vol. 36,p. 3125 - 3129

* For details of the synthesis route, please refer to the original source to ensure accuracy.