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78314-63-3

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78314-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78314-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78314-63:
(7*7)+(6*8)+(5*3)+(4*1)+(3*4)+(2*6)+(1*3)=143
143 % 10 = 3
So 78314-63-3 is a valid CAS Registry Number.

78314-63-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyloxypropionaldehyde diethyl acetal

1.2 Other means of identification

Product number -
Other names 3-benzyloxy-1-propanal diethyl acetal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78314-63-3 SDS

78314-63-3Relevant articles and documents

Synthesis and antiviral evaluation of 1′-branched-5′- norcarbocyclic adenosine phosphonic acid analogues

Oh, Chang Hyun,Yoo, Kyung Ho,Hong, Joon Hee

experimental part, p. 2473 - 2478 (2010/11/19)

Novel 1′-methyl-5′-norcarbocyclic adenosine phosphonic acid analogues were synthesized using an acyclic stereoselective route from commercially available 3,3-diethoxy-propan-1-ol 4. The synthesized nucleoside phosphonate 19 and phosphonic acid 21 were sub

Stereocontrolled Preparation of Cyclic Xanthate; a Novel Synthetic Route to 4-Thiofuranose and 4'-Thionucleoside

Uenishi, Jun'ichi,Motoyama, Mitsuhiro,Nishiyama, Yoshitaka,Wakabayashi, Shoji

, p. 1421 - 1422 (2007/10/02)

Optically active cyclic xanthate was prepared by the reaction of an epoxy alcohol with NaH and CS2, and was found to be a useful intermediate for synthesis of 4-thio-2-deoxyribose and 4'-thio-2'-deoxyribonucleoside.

CHEMICAL STUDIES ON TUBERACTINOMYCIN. XVIII. SYNTHESES OF DL-DIHYDROVIOMYCIDINE AND DL-VIOMYCIDINE

Wakamiya, Tateaki,Konishi, Kunikazu,Chaki, Haruyuki,Teshima, Tadashi,Shiba, Tetsuo

, p. 999 - 1005 (2007/10/02)

Dihydroviomycidine (2) and viomycidine (3) were guanidino amino acids derived artificially from tuberactidine (1) in peptide antibiotics tuberactinomycin A and B (viomycin).The amino acids 2 and 3 of DL-forms were synthesized from common precursor, threo-

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