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5-hydroxymethyl-1,2,3,4-cyclohexanetetrol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95043-48-4

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95043-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95043-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,4 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95043-48:
(7*9)+(6*5)+(5*0)+(4*4)+(3*3)+(2*4)+(1*8)=134
134 % 10 = 4
So 95043-48-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O5/c8-2-3-1-4(9)6(11)7(12)5(3)10/h3-12H,1-2H2/t3-,4+,5-,6+,7+/m1/s1

95043-48-4Relevant academic research and scientific papers

A norbornyl route to cyclohexitols: Structural diversity in fragmentation through functional group switching. Synthesis of α- and β- galactose, α-talose and α-fucopyranose carbasugars

Mehta, Goverdhan,Mohal, Narinder,Lakshminath, Sripada

, p. 3505 - 3508 (2007/10/03)

A novel fragmentation sequence has been executed within the norbornane system, involving C1-C7 bond scission, to extract a versatile, highly functionalized cyclohexanoid moiety. Its further evolution towards a range-of carbasugars is described. (C) 2000 Elsevier Science Ltd.

Strain-Directed Bridge Cleavage of (Phenylsulfonyl)-7-oxabicycloheptane Derivatives: Application to the Total Synthesis of Carba-α-DL-glucopyranose

Acena, Jose Luis,Arjona, Odon,Pradilla, Roberto Fernandez de la,Plumet, Joaquin,Viso, Alma

, p. 1945 - 1946 (2007/10/02)

New methodology to prepare highly oxygenated cyclohexenylsulfones by regioselective β-elimination of (phenylsulfonyl)-7-oxabicycloheptane derivatives has been developed, and its application to the total synthesis of carba-α-DL-glucopyranose is desc

SYNTHESIS OF FOUR NEW DIASTEREOISOMERS OF DL-5-HYDROXYMETHYL-1,2,3,4-CYCLOHEXANETETROL

Ogawa, Seiichiro,Tsukiboshi, Yoshiki,Iwasawa, Yoshikazu,Suami, Tetsuo

, p. 77 - 90 (2007/10/02)

Four new diastereoisomers of the pseudo-sugar DL-5-hydroxymethyl-1,2,3,4-cyclohexanetetrol, having (1,2,3,4/5)- (2), (1,5/2,3,4)- (3), (1,2,3/4,5)- (4), and (1,2,4,5/3)-configurations (5), have been synthesised by unambiguous sequences from readily availa

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