Skip to Content
Merck
CN

33735

Dibenzyl N,N-diisopropylphosphoramidite

purum, ≥97.0% (CHN)

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
[(CH3)2CH]2NP(OCH2C6H5)2
CAS Number:
Molecular Weight:
345.42
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
3616864
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


grade

purum

assay

≥97.0% (CHN)

refractive index

n20/D 1.535 (lit.)

bp

130 °C/0.55 mmHg (lit.)

density

1.028 g/mL at 25 °C (lit.)

SMILES string

CC(C)N(C(C)C)P(OCc1ccccc1)OCc2ccccc2

InChI

1S/C20H28NO2P/c1-17(2)21(18(3)4)24(22-15-19-11-7-5-8-12-19)23-16-20-13-9-6-10-14-20/h5-14,17-18H,15-16H2,1-4H3

InChI key

ANPWLBTUUNFQIO-UHFFFAOYSA-N

Other Notes

Phosphitylating agent used in the synthesis of benzyl esters of inositol phosphates from inositols


Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



W Tegge et al.
Proceedings of the National Academy of Sciences of the United States of America, 86(1), 94-98 (1989-01-01)
Chiral inositols (D-chiro-inositol from D-pinitol and L-chiro-inositol from L-quebrachitol) were converted to the 3,4-di-O-benzyl ethers, which were selectively benzoylated to yield the 1,2,5-tri-O-benzoyl-3,4-di-O-benzyl-chiro-inositols. The free hydroxyl group in each derivative was inverted by way of the trifluoromethane sulfonate ester to
K.K. Reddy et al.
Tetrahedron Letters, 34, 7869-7869 (1993)