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DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE

Product Name
DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE
CAS No.
122194-07-4
Chemical Name
DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE
Synonyms
dimethyl diisopropylphosphoramidite;DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE;DIMETHYL-N,N-DIISOPROPYLPHOSPHOROAMIDITE;Dimethyl N,N-diisopropylphosphoramidite >=95.0% (GC);Dimethyl N,N-diisopropylphosphoramidite;Phosphoramidous acid, N,N-bis(1-methylethyl)-, dimethyl ester
CBNumber
CB8440943
Molecular Formula
C8H20NO2P
Formula Weight
193.22
MOL File
122194-07-4.mol
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DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Property

Boiling point:
54 °C10 mm Hg(lit.)
Density 
0.840 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.420(lit.)
Flash point:
100 °C
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
Chloroform (Sparingly), Ethyl Acetate (Sparingly)
form 
Oil
color 
Clear Colourless
Stability:
Moisture Sensitive
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
10-21
HS Code 
2929 90 00
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

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

P302+P352IF ON SKIN: wash with plenty of soap and water.

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

TRC
Product number
D472500
Product name
Dimethyl N,N-diisopropylphosphoramidite
Packaging
5g
Price
$185
Updated
2021/12/16
Biosynth Carbosynth
Product number
FD22252
Product name
Dimethyl N,N-diisopropylphosphoramidite
Packaging
10g
Price
$275
Updated
2021/12/16
Ark Pharm
Product number
AK186440
Product name
Dimethyl N,N-diisopropylphosphoramidite
Purity
97%
Packaging
5g
Price
$293
Updated
2021/12/16
Apolloscientific
Product number
OR963457
Product name
Dimethyl N,N-diisopropylphosphoramidite
Purity
97%
Packaging
5g
Price
$363
Updated
2021/12/16
AK Scientific
Product number
Z8605
Product name
Dimethyl N,N-diisopropylphosphoramidite
Packaging
10g
Price
$549
Updated
2021/12/16
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DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Chemical Properties,Usage,Production

Uses

A useful reagent for the efficient phosphorylation of alcohols.

reaction suitability

reaction type: Phosphorylations

Synthesis

67-56-1

921-26-6

122194-07-4

General procedure for the synthesis of dimethyl N,N-diisopropylphosphoramidite amide from methanol and dichloro-N,N-diisopropylphosphoramidite: firstly, the yellow solution obtained from the reaction was subjected to rotary evaporation, followed by the direct addition of 47 mL (325 mmol, 32.9 g) of triethylamine and 250 mL of tetrahydrofuran, and stirring of the mixture to obtain a yellow suspension. Anhydrous methanol 13 mL (322 mmol, 10.3 g) was prepared in a dropping funnel, and methanol was slowly added dropwise to the reaction system over a period of 20 min under nitrogen protection and an ice-salt bath, and the dropping funnel was washed with 150 mL of tetrahydrofuran. Upon completion of the dropwise addition, the reaction mixture was transformed into a white suspension. The ice bath was removed and stirring was continued for 2 h. The reaction was then allowed to stand for a few minutes and diafiltration was performed to obtain a yellow liquid containing a light pink solid. The solid was washed with a small amount of tetrahydrofuran. The tetrahydrofuran was removed by rotary evaporation. The product was dissolved in 10 mL of 5% sodium bicarbonate solution and extracted three times with 20 mL of dichloromethane, the organic phases were combined, the dichloromethane was removed by rotary evaporation, and finally a reduced pressure distillation was performed to collect 78 stable fractions. A colorless liquid and a white solid were observed in the condenser tube, which were identified as the same substance, and the collections could be combined to give a final yield of 16.68 g with 42% yield.

References

[1] Journal of the Chemical Society. Perkin Transactions 2, 1998, # 7, p. 1621 - 1628
[2] Patent: CN102977145, 2017, B. Location in patent: Paragraph 0184; 0185

DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Preparation Products And Raw materials

Raw materials

Preparation Products

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DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE Suppliers

3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
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86-21-50328109
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3bsc@sina.com
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China
ProdList
15838
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69
Beijing Ouhe Technology Co., Ltd
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010-010-82967028 13522913783
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+86-10-82967029
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2355560935@qq.com
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China
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12000
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Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
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shchemsky@sina.com
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China
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32321
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9ding chemical ( Shanghai) Limited
Tel
4009209199
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86-021-52271987
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sales@9dingchem.com
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China
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18209
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Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
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China
ProdList
39966
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Shenzhen Nexconn Pharmatechs Ltd.
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0755-89396905
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admin@nexconn.com
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China
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Sigma-Aldrich
Tel
021-61415566 800-8193336
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orderCN@merckgroup.com
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China
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51395
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Zhengzhou Acme Chemical Co., Ltd.
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0371-0371-55629727 13323845623
Fax
037155629727
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2885676761@qq.com
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China
ProdList
10110
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LinkChem Technology Co., Ltd.
Tel
021-58950110 13124863828
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021-20922272
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sales@linkchem.cn
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China
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2998
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Shanghai Thoreco Novel Material Co. Ltd
Tel
021-34202258 17317865669;
Email
Sales@thoreco.com
Country
China
ProdList
183
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View Lastest Price from DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE manufacturers

Career Henan Chemical Co
Product
DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE 122194-07-4
Price
US $0.01/KG
Min. Order
1KG
Purity
95%-99%
Supply Ability
1kg; 100kg; 500kg
Release date
2019-12-24

122194-07-4, DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITERelated Search:


  • DIMETHYL N,N-DIISOPROPYLPHOSPHORAMIDITE
  • DIMETHYL-N,N-DIISOPROPYLPHOSPHOROAMIDITE
  • Dimethyl N,N-diisopropylphosphoramidite >=95.0% (GC)
  • Phosphoramidous acid, N,N-bis(1-methylethyl)-, dimethyl ester
  • dimethyl diisopropylphosphoramidite
  • Dimethyl <i>N</i>,<i>N</i>-diisopropylphosphoramidite
  • 122194-07-4
  • C8H20NO2P
  • Phosphoramidites
  • Phosphorus Compounds
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  • Organic Building Blocks
  • Phosphoramidites
  • Phosphorus Compounds