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2-(Tributylstannyl)pyrimidine

Product Name
2-(Tributylstannyl)pyrimidine
CAS No.
153435-63-3
Chemical Name
2-(Tributylstannyl)pyrimidine
Synonyms
SKL1126;2-tributyltinpyrMidine;2-(tributyltin) pyrimidine;-(Tributylstannyl)pyrimidine;Tributyl(2-pyrimidyl)stannane;2-(Tributylstannanyl)pyrimidine;PyriMidine,2-(tributylstannyl)-;ributyl(pyrimidin-2-yl)stannane;2-(tri-n-butylstannyl)pyrimidine;(Pyrimidin-2-yl)tributylstannane
CBNumber
CB81177116
Molecular Formula
C16H30N2Sn
Formula Weight
369.13
MOL File
153435-63-3.mol
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2-(Tributylstannyl)pyrimidine Property

Boiling point:
381.2±25.0 °C(Predicted)
Density 
1.164 g/mL at 25 °C
refractive index 
n20/D1.512
Flash point:
>110℃
storage temp. 
Sealed in dry,2-8°C
solubility 
soluble in Methanol; Ethyl Acetate; Dichloromethane; Chloroform; DMF; DMSO
form 
liquid
pka
1.42±0.33(Predicted)
color 
Colourless
InChI
InChI=1S/C4H3N2.3C4H9.Sn/c1-2-5-4-6-3-1;3*1-3-4-2;/h1-3H;3*1,3-4H2,2H3;
InChIKey
WTFFOOAJSDVASL-UHFFFAOYSA-N
SMILES
C1([Sn](CCCC)(CCCC)CCCC)=NC=CC=N1
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Safety

Hazard Codes 
Xi,T,N
Risk Statements 
21-25-36/38-48/23/25-50/53
Safety Statements 
36/37/39-45-60-61-35
RIDADR 
UN 2788 6.1 / PGIII
WGK Germany 
3
HazardClass 
IRRITANT, TOXIC, KEEP COLD
HS Code 
29339900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H312Harmful in contact with skin

H315Causes skin irritation

H319Causes serious eye irritation

H372Causes damage to organs through prolonged or repeated exposure

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P202Do not handle until all safety precautions have been read and understood.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
721174
Product name
2-(Tributylstannyl)pyrimidine
Purity
95%
Packaging
1g
Price
$146.3
Updated
2025/07/31
Sigma-Aldrich
Product number
721174
Product name
2-(Tributylstannyl)pyrimidine
Purity
95%
Packaging
5g
Price
$245
Updated
2025/07/31
TRC
Product number
T773988
Product name
2-(Tributylstannyl)pyrimidine
Packaging
2.5g
Price
$385
Updated
2021/12/16
SynQuest Laboratories
Product number
9H50-1-X8
Product name
2-(Tributylstannyl)pyrimidine
Purity
97%
Packaging
250mg
Price
$35
Updated
2021/12/16
Oakwood
Product number
043836
Product name
2-Tributylstannylpyrimidine
Purity
95%
Packaging
250mg
Price
$40
Updated
2021/12/16
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2-(Tributylstannyl)pyrimidine Chemical Properties,Usage,Production

Chemical Properties

Clear colorless liquid

Uses

2-(Tributylstannyl)pyrimidine is an organotin compound used in Stille coupling reaction. This can be used as one of the precursors in the synthesis of 2-aminopyridine oxazolidinones as potent and selective tankyrase (TNKS) inhibitors and the synthesis of canagliflozin, a novel inhibitor for sodium-dependent glucose cotransporter.
It can also be used in the preparation of various (2-pyrimidyl)silanes.

Synthesis

1722-12-9

688-73-3

153435-63-3

Under nitrogen protection, tributyltin hydride (12.5 g) was dissolved in 20 mL of anhydrous tetrahydrofuran in a round bottom flask. With stirring at 0 °C, 2M lithium diisopropylammonium (18.75 g) was slowly added with continuous stirring for 30 min. Subsequently, the reaction system was cooled to -18 °C and 2-chloropyrimidine (4 g, 35 mmol) dissolved in 20 mL of anhydrous tetrahydrofuran was slowly added dropwise. After the dropwise addition, the reaction system was gradually warmed to room temperature and stirring was continued for 12 hours. Upon completion of the reaction, the reaction was quenched by the addition of 30 mL of water and extracted with ethyl acetate. The organic phases were combined, concentrated under reduced pressure to remove the solvent, and finally purified by column chromatography to afford 2-(tributyltin)pyrimidine (11.68 g, 90% yield).

References

[1] Patent: KR2018/75381, 2018, A. Location in patent: Paragraph 0071; 0072-0074
[2] Patent: EP1724268, 2006, A1. Location in patent: Page/Page column 58; 77; 95

2-(Tributylstannyl)pyrimidine Preparation Products And Raw materials

Raw materials

Preparation Products

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2-(Tributylstannyl)pyrimidine Suppliers

Chengdu Aslee Biopharmaceuticals, Inc
Tel
028-85305008 02885305008
Fax
4000210878-186
Email
2306208234@qq.com
Country
China
ProdList
1006
Advantage
50
Aikon International Limited
Tel
025-58859352 18068836627
Fax
02557626880
Email
sales01@aikonchem.com
Country
China
ProdList
15083
Advantage
58
Yangzhou beierdun new material technology co., ltd
Tel
13776432722
Email
358854490@qq.com
Country
China
ProdList
39
Advantage
58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Chang Zhou Chemistar Chemistry Technology Co.,Ltd
Tel
+86 (519) 8689-6136
Fax
+86 (519) 8205-9235
Email
kr@krchemistar.com
Country
China
ProdList
181
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Accela ChemBio Co.,Ltd.
Tel
021-50795510 4000665055
Fax
021-50795055
Email
sales@accelachem.com
Country
China
ProdList
11035
Advantage
64
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Fax
+86-25-83453306
Email
info@chemlin.com.cn
Country
China
ProdList
15883
Advantage
64
Shandong Xiya Chemical Co., Ltd
Tel
4009903999 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18729
Advantage
57
Shanghai Ennopharm Co., Ltd.
Tel
+86 (21) 6435-5022
Country
China
ProdList
4267
Advantage
65
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View Lastest Price from 2-(Tributylstannyl)pyrimidine manufacturers

Career Henan Chemical Co
Product
2-(Tributylstannyl)pyrimidine 153435-63-3
Price
US $2.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
100g , 1kg, 5kg , 50kg
Release date
2020-01-07

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