| Company Name: |
Energy Chemical
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| Tel: |
021-021-58432009 400-005-6266 |
| Email: |
sales8178@energy-chemical.com |
| Products Intro: |
Product Name:(R)-(+)-α-Acetoxyphenylacetonitrile
CAS:119718-89-7
Purity:99% Package:250MG,250MG
|
| Company Name: |
VDM Biochemicals
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| Tel: |
0330-2528181 |
| Email: |
sales@vdmbio.com |
| Products Intro: |
Product Name:(R)-α-Acetoxyphenylacetonitrile
CAS:119718-89-7
Purity:>=97%
|
| Company Name: |
Sigma-Aldrich
|
| Tel: |
021-61415566 800-8193336 |
| Email: |
orderCN@merckgroup.com |
| Products Intro: |
Product Name:(R)-alpha-Acetoxyphenylacetonitrile
CAS:119718-89-7
Purity:>=97.0% (sum of enantiomers, GC) Package:1ML Remarks:00873-1ML
|
| Company Name: |
Merck KGaA
|
| Tel: |
21-20338288 |
| Email: |
ordercn@merckgroup.com |
| Products Intro: |
Product Name:(R)-α-Acetoxyphenylacetonitrile
CAS:119718-89-7
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| Company Name: |
Santa Cruz Biotechnology Inc
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| Tel: |
021-60936350 |
| Email: |
scbt@scbt.com |
| Products Intro: |
Product Name:(R)-α-Acetoxyphenylacetonitrile, CAS 119718-89-7
CAS:119718-89-7
|
|
| | (R)-ALPHA-CYANOBENZYL ACETATE Basic information |
| Product Name: | (R)-ALPHA-CYANOBENZYL ACETATE | | Synonyms: | D-MANDELONITRILE ACETATE;(r)-α-cyanobenzyl acetate;(R)-α-Cyanobenzyl acetate, O-Acetyl-D-mandelonitrile;(R)-ALPHA-CYANOBENZYL ACETATE;(R)-(+)-ALPHA-ACETOXYPHENYLACETONITRILE;(R)-ALPHA-ACETOXYPHENYLACETONITRILE;O-ACETYL-D-MANDELONITRILE;Benzeneacetonitrile, α-(acetyloxy)-, (αR)- | | CAS: | 119718-89-7 | | MF: | C10H9NO2 | | MW: | 175.18 | | EINECS: | | | Product Categories: | Chiral building block | | Mol File: | 119718-89-7.mol |  |
| | (R)-ALPHA-CYANOBENZYL ACETATE Chemical Properties |
| Boiling point | 268 °C(lit.) | | density | 1.115 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.506 | | Fp | >230 °F | | Optical Rotation | [α]20/D +8.0±0.5°, c =10% in chloroform |
| | (R)-ALPHA-CYANOBENZYL ACETATE Usage And Synthesis |
| Uses | (R)-α-Acetoxyphenylacetonitrile can be used as a model compound in the iodine promoted as well as t-BuONO-assisted secondary amides synthesis via an aryl?N-addition reaction to the -CN group of nitriles. |
| | (R)-ALPHA-CYANOBENZYL ACETATE Preparation Products And Raw materials |
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